Poland - Reagents and contrast media

Description

REAL TIME PCR PCR reagents based on Real TIME PCR TECHNOLOGY COMPliant with COBAS® 4800 HIV RNA VIREMIAL LEVEL TECHNOLOGY Ordering Party requires offering reagents and all components - a complete diagnostic kit to isolate genomic nucleic acids for full result and interchangeable materials (disposable plastics) necessary to perform the test, along with calibration and internal controls to provide 8520 effective results. Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature. REAGENTS BASED ON REAL TIME PCR REAL TECHNOLOGY WITH COBAS® AmpliPrep and COBAS® TaqMan 48 APARTMENTS FOR VIREMIAL LEVEL CONTROLS HIV RNA.The customer requires all reagents and components - a complete diagnostic kit to isolate genomic nucleic acids for the full result and replaceable materials (disposable plastics) needed to perform the test, along with calibration and internal control to produce a total of 7266 effective results. Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature. The purchaser requires a complete diagnostic kit for isolating genomic nucleic acids for the full result and the replaceable materials (disposable plastics) needed to perform the test, along with calibration and internal control to produce a total of 4130 effective reagents and all components - a complete diagnostic kit for isolating genomic nucleic acids for the full result and the replaceable materials (disposable plastics) needed to perform the test, along with calibration and internal control to produce a total of 4130 effective, effective, single-use plastics.Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature. REAL TIME PCR REAGENTS BASED ON REAL TIME PCR TECHNOLOGY COMPliant with m2000rt™ and m2000sp™ or COBAS® AmpliPrep and COBAS® TaqMan 48 TO TEST THE VIREMIAL LEVEL HIV RNA.The customer requires all reagents and components - a complete diagnostic kit to isolate genomic nucleic acids for the full result and replaceable materials (disposable plastics) needed to perform the test, along with calibration and internal control to produce a total of 8820 effective results. Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature. The Principal requires that we offer a set of medical devices and all components necessary to achieve a total of 792 effective results for reverse transcriptase inhibitors and protease inhibitors. If it results from the test design, which is confirmed by the relevant provision in the instruction manual, the Contracting Authority allows for offering medical devices that allow simultaneous obtaining of two independent results for the presence of reverse transcriptase inhibitors and protease inhibitors during one test, using one test. Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Contractor in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature. HIV GENOTICAL RESISTANCE READERS FOR LEKOOPORNITY - ALL CHILDREN'S ORDERS require a set of medical devices and all components necessary to achieve a total of 1305 effective results in the range of reverse transcriptase and protease inhibitors. If it results from the test design, which is confirmed by the relevant provision in the instruction for use, the Contracting Authority allows for offering tests that allow simultaneous obtaining of two independent results for the presence of reverse transcriptase inhibitors and protease inhibitors during one test, using one test. Pursuant to § 13 section 1 item 3 of the Regulation of the Minister of Development of 26 July 2016 on the types of documents that the Contracting Authority may request from the Contractor in the procurement procedure (Journal of Laws of 27 July 2016, item 1126), in connection with the Regulation of the Minister of Enterprise and Technology of 16 October 2018 amending the Regulation on the types of documents that the Contracting Authority may request from the Economic Operator in the procurement procedure - Journal of Laws of 17 October 2018, In order to confirm that the offered deliveries meet the requirements specified by the Ordering Party, the Economic Operator is obliged to submit with the offer copies of appropriate documents confirming the fulfilment of the subjective conditions specified in each part (e.g. instructions for use, description of the marking methodology). The documents referred to above are submitted in the form of an original electronic document or a copy certified for conformity with the original by the Economic Operator with the use of a qualified electronic signature.

Opportunity closing date

22 August 2019

Value of contract

to be confirmed