Zakup i sukcesywna dostawa produktu leczniczego - BOSENTANUM

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The quality requirements for medicinal products are specified in the Act of September 6, 2001 - Pharmaceutical Law (consolidated text Journal of Laws of 2016, item 2142, as amended), which in Article 1, paragraph 1, point 1 states that it defines, among others, the principles and procedures for admission of medicinal products to the market, taking into particular account the requirements concerning the quality, efficacy, and safety of their use. Furthermore, the Regulation of the Minister of Health of November 9, 2015 on the requirements of Good Manufacturing Practice (Journal of Laws 2015, item 1979) specifies in detail the requirements to ensure appropriate quality of the medicinal product. In the present procedure, the quality standard of medicinal products has been defined by the Contracting Authority by providing in the description of the subject of the contract, which includes among others: composition, form and route of administration, and unit of measure. The quality requirements for medicinal products are specified in the Act of September 6, 2001 - Pharmaceutical Law (consolidated text Journal of Laws of 2016, item 2142, as amended), which in Article 1, paragraph 1,…

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