The subject of the contract is the supply of reagents for DNA and RNA analysis together with mats. labor. and sequencing reagents. The order was divided into 3 parts. An offer can be made for all parts. A detailed description and method of order execution are included in the assortment and price table of Appendix No. 2 to the Terms of Use and the model agreement of Appendices No. 4 and 4a to the Terms of Reference. The deadline for the completion of the order is: 24 months for part II. 1 and 12 months for part II Nos 2 and 3 from the date of conclusion of the contract. The Contracting Authority declares that being the data controller and taking into account the provisions of the Act of 10.05.2018 on the protection of personal data, it has implemented security measures adequate to the risks identified by it and providing a guarantee of proper protection of personal data transferred as part of the procedure. Detailed info clause. Article 13 of the GDPR contained in the Terms of Reference. The Contracting Authority does not require the payment of a bid bond. The Contracting Authority does not provide for the award of contracts referred to in Article 214(1)(8) of the Public Procurement Law.

Supply of reagents for DNA and RNA analysis along with laboratory materials. A detailed description and method of order execution are included in the assortment and price table of Appendix No. 2 to the Terms of Use and a model agreement attached No. 4 to the Terms of Reference. The Contracting Authority requires that the following means of evidence be submitted together with the offer, under pain of nullity, to confirm that the offered supplies meet the requirements specified by the Contracting Authority: 1) A valid document confirming that it has been approved for marketing and use as a medical device that meets the requirements within the meaning of the Act of 7.04.2022 on medical devices (Journal of Laws of 2022, item 974) and Directive 93/42/EEC or compliance with Regulation (EU) of the European Parliament and of the European Parliament Regulation (EU) 2017/745 of the European Parliament and of the Council on Medical Devices (MDR) / (EU) 2017/46 on in vitro medical devices, bearing the CE mark on the device - i.e.: a declaration of conformity / certificate of conformity issued by the manufacturer or an authorized/authorized representative confirming that the device complies with the essential requirements. or: Contractor's statement confirming that the offered products meet the requirements specified by the Ordering Party and are approved for marketing and use in Polish in accordance with applicable regulations if the subject of the contract described in the Terms of Reference has not been classified as a medical device. 2) Information materials containing a description of the offered subject of the contract (prospectus, catalogue, card, data form, etc.), confirming the requirements contained in Appendix No. 2 to the Terms of Reference (indicating the required parameters, part number and position of the offered subject of the contract).

2.If the Contractor does not submit the measures of evidence in question or the measures in question are incomplete, the Contracting Authority shall call for their submission or supplement within the time limit set.

Supply of sequencing reagents. A detailed description and method of order execution are included in the assortment and price table of Appendix No. 2 to the Terms of Use and a model agreement attached No. 4 to the Terms of Reference. The Contracting Authority requires that the following means of evidence be submitted together with the offer, under pain of nullity, in electronic form to confirm that the offered supplies meet the requirements specified by the Contracting Authority: 1) A valid document confirming that it has been approved for marketing and for use as a medical device that meets the requirements within the meaning of the Act of 7.04.2022.

on medical devices (Journal of Laws of 2022, item 974) and Directive 93/42/EEC or compliance with Regulation (EU) 2017/745 of the European Parliament and of the Council on Medical Devices (MDR) / (EU) 2017/46 on in vitro medical devices, having the product marking with the CE mark - i.e.: declaration of conformity / certificate of conformity issued by the manufacturer or an authorized/authorized representative confirming that the device complies with the essential requirements. or: Contractor's statement confirming that the offered products meet the requirements specified by the Ordering Party and are approved for marketing and use in Polish in accordance with applicable regulations if the subject of the contract described in the Terms of Reference has not been classified as a medical device. 2) Information materials containing a description of the offered subject of the contract (prospectus, catalogue, card, data form, etc.), confirming the requirements contained in Appendix No. 2 to the Terms of Reference (indicating the required parameters, part number and position of the offered subject of the contract).

2.If the Contractor does not submit the measures of evidence in question or the measures in question are incomplete, the Contracting Authority shall call for their submission or supplement within the time limit set.

Supply of sequencing reagents as part of the DINO project. A detailed description and method of order execution are included in the assortment and price table of Appendix No. 2 to the Terms of Use and a model contract of Appendix No. 4a to the Terms of Reference. The Contracting Authority requires that the following means of evidence be submitted together with the offer, under pain of nullity, in electronic form to confirm that the offered supplies meet the requirements specified by the Contracting Authority: 1) A valid document confirming that it has been approved for marketing and for use as a medical device that meets the requirements within the meaning of the Act of 7.04.2022.

on medical devices (Journal of Laws of 2022, item 974) and Directive 93/42/EEC or compliance with Regulation (EU) 2017/745 of the European Parliament and of the Council on Medical Devices (MDR) / (EU) 2017/46 on in vitro medical devices, having the product marking with the CE mark - i.e.: declaration of conformity / certificate of conformity issued by the manufacturer or an authorized/authorized representative confirming that the device complies with the essential requirements. or: Contractor's statement confirming that the offered products meet the requirements specified by the Ordering Party and are approved for marketing and use in Polish in accordance with applicable regulations if the subject of the contract described in the Terms of Reference has not been classified as a medical device. 2) Information materials containing a description of the offered subject of the contract (prospectus, catalogue, card, data form, etc.), confirming the requirements contained in Appendix No. 2 to the Terms of Reference (indicating the required parameters, part number and position of the offered subject of the contract).

2.If the Contractor does not submit the measures of evidence in question or the measures in question are incomplete, the Contracting Authority shall call for their submission or supplement within the time limit set.