Pharmaceutical products | Tenderlake

Pharmaceutical products

Contract Value:
PLN 36M - 36M
Notice Type:
Contract Notice
Published Date:
18 November 2022
Closing Date:
21 December 2022
Location(s):
PL911 Miasto Warszawa (PL Poland/POLSKA)
Description:
Supply of medicinal products for chemotherapy, drug programs

Supply of medicinal products for chemotherapy, drug programs

purchase and supply of Vedolizumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Bicalutamid

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product urapidyl

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Cyclosporin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of ONS diets

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of ons ons part 2

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Meropenem

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products everolimus

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of ONS diets part 3

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

Purchase and successive delivery of Vaccines

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Zoledronic acid

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Parikalcytol

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Aflibercept

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Cisplatinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Paclitaxel

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Sorafenib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of ribociclib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product dimethyl fumarate

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product darbepoietin alfa

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Durvalumabum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Epoetinum alfa

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Lanreotide

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product oxaliplatin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Gemcitabinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products Tocilizumab, obinutuzumab and others

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product peginterferon beta -1A

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Mercaptopurinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of cytarabina

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Filgrastimum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products okrelizumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Lenalidomid

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of carboplatin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Macitentan

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Natalizumab medicinal products

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of tofacitinib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Aprepitant

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Chlorambucil

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of medicinal products illoprost

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Interferonum beta -1A

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of interferon beta 1A

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Lapatinibum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Sekukinumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Darbepoetinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Aflibercept

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product ondansetron

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Ciclosporinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product teriflunomide

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Kabozantinib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Bosentanum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product folinic acid in the form of calcium folate

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Adalimumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Everolimus

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Melphelan

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Panitumumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Netupitant + palonosetron

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product imatinib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product pemetrexedum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Carfilzomib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Alektynib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product Upadacitinibum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Nintedanib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product alprostadil

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of propofolum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Abirateroni acetas

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Dexamethasone sodium phosphate inj

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Trombinum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Phenylephrine

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the product cefiderokol

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product dobutaminum

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product drotaverine i.v.

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Gadobenic acid

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of potable substances

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of cefepime

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Metronidazole i.v.

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Palbocylib

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product fosfomycin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

Purchase and successive delivery of medicinal products

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

Purchase and Successive Delivery of Argipresine

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product fibrinogen

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product protamine sulphate

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product fluconazole

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Antithrombin III

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product thiamine

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of the medicinal product short-acting insulin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product insulin analogues

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of trastuzumab

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product analogue of fast-acting insulin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product insulin analogue c.d

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the insulin analogue medicinal product

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Imipenem with cilastin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of a medicinal product

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Amikacin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Kaspofungin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products allergen extract of fibrowing insects

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Paracetamol I.V.

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product cisatracurium

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product peginterferon alfa -2A

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product ceftasidym + awibaktam

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of Vancomycin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product - tissue glue

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product potasium chloride inj

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product fibrinogen + thrombin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products of membrane-winged insect venom for tests and non-specific immunotherapy

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of medicinal products for parenteral nutrition

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive supply of medicinal products vancomycin for intravenous and oral supply

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product Suxamehtonium chloride

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

purchase and successive delivery of the medicinal product rifaximin

The quality requirements of medicinal products are specified in the Act of 6 September 2001 - Pharmaceutical Law (i.e. Journal of Laws of 2020, item 944), which in Art. Article 1(1)(1) provides that it lays down, m.in, the rules and procedures for the authorisation of medicinal products, taking into account, in particular, the requirements relating to the quality, efficacy and safety of their use.' In addition, the Regulation of the Minister of Health of 9 November 2015 on the requirements of Good Manufacturing Practice (Journal of Laws of 2019, item 728 of późn.zm) specifies in detail the requirements for ensuring the appropriate quality of the medicinal product. In the proceedings in question, the quality requirements of medicinal products have been defined by the Ordering Party by specifying in the description of the subject of the contract which includes, m.in. composition, form and route of administration and unit of measurement.

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The Buyer:
Centralny Szpital Kliniczny Ministerstwa Spraw Wewnętrznych i Administracji w Warszawie
CPV Code(s):
09221100 - Petroleum jelly
15880000 - Special nutritional products
15882000 - Dietetic products
24313300 - Carbonates
33600000 - Pharmaceutical products
33612000 - Medicinal products for functional gastrointestinal disorders
33614000 - Antidiarrhoeals, intestinal anti-inflammatory/anti-infective agents
33615100 - Insulin
33616000 - Vitamins
33621100 - Antithrombotic agents
33621200 - Antihaemorrhagics
33621300 - Antianaemic preparations
33621400 - Blood substitutes and perfusion solutions
33622100 - Cardiac therapy medicinal products
33622200 - Antihypertensives
33631600 - Antiseptics and disinfectants
33632000 - Medicinal products for the musculo-skeletal system
33632200 - Muscle relaxants
33642000 - Systemic hormonal preparations, excl. sex hormones
33642100 - Pituitary, hypothalamic hormones and analogues
33642200 - Corticosteroids for systemic use
33651100 - Antibacterials for systemic use
33651200 - Antimycotics for systemic use
33651610 - Diphtheria-pertussis-tetanus vaccines
33652000 - Antineoplastic and immunomodulating agents
33652100 - Antineoplastic agents
33652200 - Endocrine therapy medicinal products
33652300 - Immunosuppressive agents
33661100 - Anaesthetics
33661200 - Analgesics
33661500 - Psycholeptics
33674000 - Cough and cold preparations
33690000 - Various medicinal products
33695000 - All other non-therapeutic products
33696000 - Reagents and contrast media