Supply of medicinal products for chemotherapy, drug programs
purchase and supply of VedolizumabThe 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 BicalutamidThe 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 urapidylThe 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 CyclosporinThe 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 dietsThe 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 2The 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 MeropenemThe 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 everolimusThe 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 3The 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 VaccinesThe 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 acidThe 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 ParikalcytolThe 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 AfliberceptThe 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 CisplatinumThe 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 PaclitaxelThe 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 SorafenibThe 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 ribociclibThe 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 fumarateThe 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 alfaThe 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 DurvalumabumThe 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 alfaThe 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 LanreotideThe 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 oxaliplatinThe 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 GemcitabinumThe 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 othersThe 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 -1AThe 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 MercaptopurinumThe 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 cytarabinaThe 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 FilgrastimumThe 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 okrelizumabThe 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 LenalidomidThe 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 carboplatinThe 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 MacitentanThe 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 productsThe 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 tofacitinibThe 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 AprepitantThe 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 ChlorambucilThe 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 illoprostThe 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 -1AThe 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 1AThe 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 LapatinibumThe 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 SekukinumabThe 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 DarbepoetinumThe 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 AfliberceptThe 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 ondansetronThe 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 CiclosporinumThe 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 teriflunomideThe 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 KabozantinibThe 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 BosentanumThe 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 folateThe 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 AdalimumabThe 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 EverolimusThe 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 MelphelanThe 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 PanitumumabThe 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 + palonosetronThe 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 imatinibThe 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 pemetrexedumThe 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 CarfilzomibThe 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 AlektynibThe 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 UpadacitinibumThe 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 NintedanibThe 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 alprostadilThe 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 propofolumThe 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 acetasThe 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 injThe 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 TrombinumThe 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 PhenylephrineThe 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 cefiderokolThe 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 dobutaminumThe 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 acidThe 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 substancesThe 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 cefepimeThe 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 PalbocylibThe 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 fosfomycinThe 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 productsThe 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 ArgipresineThe 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 fibrinogenThe 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 sulphateThe 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 fluconazoleThe 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 IIIThe 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 thiamineThe 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 insulinThe 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 analoguesThe 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 trastuzumabThe 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 insulinThe 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.dThe 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 productThe 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 cilastinThe 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 productThe 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 AmikacinThe 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 KaspofunginThe 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 insectsThe 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 cisatracuriumThe 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 -2AThe 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 + awibaktamThe 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 VancomycinThe 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 glueThe 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 injThe 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 + thrombinThe 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 immunotherapyThe 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 nutritionThe 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 supplyThe 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 chlorideThe 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 rifaximinThe 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.