Poland - Antivirals for systemic use

Description

1. international chemical name of the medicinal product: Lamivudine/ZidovudinePower or volume: 150/300 mgCapacity: 150/300 mgFarm: tabletPack size 60 pieces.Number of packages: 2.1 Pursuant to § 13 item 1 point 3 of the Regulation of the Minister of Development of 26.7.2016 on types of documents which may be requested by the Contracting Authority from the Economic Operator in a procurement procedure - Dz. U. of 27.7.2016, item 1126, in connection with the Ordinance of the Minister of Entrepreneurship and Technology of 16.10.2018 amending the Ordinance on the types of documents that can be demanded by the Contracting Authority from the Contractor in the contract award procedure (Dz.U. of 17.10.2018, item 1993), in order to confirm that the offered supplies meet the requirements specified by the Ordering Party, the Economic Operator shall be obliged to confirm with an appropriate document, i.e. submit with the tender form (subject conditions):- a valid, current marketing authorization for the territory of the Republic of Poland issued by the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products or - a valid, current marketing authorization issued by the Council of the European Union or the European Commission.2The aforementioned documents must have a validity period covering the entire contract execution period.2.4 If a document expires, the Economic Operator shall provide the Contracting Authority with the documents referred to in item 2.1, an additional document declaring the timely submission of an application to extend the validity of the permit or, if a valid permit is obtained.2The documents referred to above shall be submitted in the form of an original electronic document or a copy certified by the Economic Operator to be true to the original with the use of a qualified electronic signature.2.6 Documents drawn up in a foreign language shall be submitted together with a translation into Polish. 1. international chemical name of the medicinal product: 30 pieces.Number of packages: 2.1 Pursuant to § 13 item 1 point 3 of the Regulation of the Minister of Development of 26.7.2016 on types of documents which may be requested by the Contracting Authority from the Economic Operator in a procurement procedure - Dz.U. of 27.7.2016, item 1126, in connection with the Ordinance of the Minister of Entrepreneurship and Technology of 16.10.2018 amending the Ordinance on the types of documents that can be demanded by the Contracting Authority from the Contractor in the contract award procedure (Dz.U. of 17.10.2018, item 1993), in order to confirm that the offered supplies meet the requirements specified by the Ordering Party, the Economic Operator shall be obliged to confirm with an appropriate document, i.e. submit with the tender form (subject conditions):- a valid, current marketing authorization for the territory of the Republic of Poland issued by the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products or - a valid, current marketing authorization issued by the Council of the European Union or the European Commission.2The aforementioned documents must have a validity period covering the entire contract execution period.2.4 If a document expires, the Economic Operator shall provide the Contracting Authority with the documents referred to in item 2.1, an additional document declaring the timely submission of an application to extend the validity of the permit or, if a valid permit is obtained.2The documents referred to above shall be submitted in the form of an original electronic document or a copy certified by the Economic Operator to be true to the original with the use of a qualified electronic signature.2.6 Documents drawn up in a foreign language shall be submitted together with a translation into Polish. 1. international chemical name of the medicinal product: 30 pieces.Number of packages: 2.1 Pursuant to § 13 item 1 point 3 of the Regulation of the Minister of Development of 26.7.2016 on types of documents which may be requested by the Contracting Authority from the Economic Operator in a procurement procedure - Dz.U. of 27.7.2016, item 1126, in connection with the Ordinance of the Minister of Entrepreneurship and Technology of 16.10.2018 amending the Ordinance on the types of documents that can be demanded by the Contracting Authority from the Contractor in the contract award procedure (Dz.U. of 17.10.2018, item 1993), in order to confirm that the offered supplies meet the requirements specified by the Contracting Authority, the Economic Operator shall be obliged to confirm with an appropriate document, i.e. submit with the tender form (subject conditions):- a valid, current marketing authorization for the territory of the Republic of Poland issued by the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products or - a valid, current marketing authorization issued by the Council of the European Union or the European Commission,2.2.Should the validity of a document expire, the Economic Operator shall provide the Contracting Authority with the documents referred to in item 2.1, an additional document declaring that the application for renewal of the permit has been submitted in due time or, if a valid permit has been obtained.2.5 The documents referred to above shall be submitted in the form of an original electronic document or a copy certified to be true to the original by the Economic Operator using a qualified electronic signature.2.6 Documents drawn up in a foreign language shall be submitted together with a translation into Polish. 1. international chemical name of the medicinal product: 30 pieces.Number of packages: 2.1 Pursuant to § 13 item 1 point 3 of the Regulation of the Minister of Development of 26.7.2016 on types of documents which may be requested by the Contracting Authority from the Economic Operator in a procurement procedure - Dz.U. of 27.7.2016, item 1126, in connection with the Ordinance of the Minister of Entrepreneurship and Technology of 16.10.2018 amending the Ordinance on the types of documents that can be demanded by the Contracting Authority from the Contractor in the contract award procedure (Dz.U. of 17.10.2018, item 1993), in order to confirm that the offered supplies meet the requirements specified by the Ordering Party, the Economic Operator shall be obliged to confirm with an appropriate document, i.e. submit with the tender form (subject conditions):- a valid, current marketing authorization for the territory of the Republic of Poland issued by the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products or - a valid, current marketing authorization issued by the Council of the European Union or the European Commission.2The aforementioned documents must have a validity period covering the entire contract execution period.2.4 If a document expires, the Economic Operator shall provide the Contracting Authority with the documents referred to in item 2.1, an additional document declaring the timely submission of an application to extend the validity of the permit or, if a valid permit is obtained.2The documents referred to above shall be submitted in the form of an original electronic document or a copy certified by the Economic Operator to be true to the original with the use of a qualified electronic signature.2.6 Documents drawn up in a foreign language shall be submitted together with a translation into Polish.

Opportunity closing date

24 February 2020

Value of contract

£100k-1m