Article 8. State Pharmacopoeia

On amendments and additions to the law of the Republic of Uzbekistan "On medicinal products and pharmaceutical activity" (LRU-399-son) · Date: 04.01.2016 · In force

The State Pharmacopoeia is an official publication consisting of a set of documents that include requirements for medicines and medical products, general pharmacopeial articles, pharmacopeial articles, and methods for quality control of medicines and medical products.

A general pharmacopeial article establishes general requirements for the quality of medicines and medical products, for medicinal plant raw materials, for methods of their quality control, for standard samples and reagents used in the quality control of medicines, and for packaging materials used in the manufacture of medicines.

A pharmacopeial article establishes requirements for the quality of a specific medicine, medical product, medicinal plant raw material, or excipient.

The development of general pharmacopeial articles and pharmacopeial articles and their inclusion in the State Pharmacopoeia shall be carried out by the Ministry of Health of the Republic of Uzbekistan in the prescribed manner.

The State Pharmacopoeia shall be published by the Ministry of Health of the Republic of Uzbekistan at least once every five years. During the period between reprints of the State Pharmacopoeia, supplements to the State Pharmacopoeia shall be published.

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Source of the text

National Database of Legislation of the Republic of Uzbekistan (lex.uz). Original on lex.uz: lex.uz/docs/6819757

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Cite as: Article 8. State Pharmacopoeia On amendments and additions to the law of the Republic of Uzbekistan "On medicinal products and pharmaceutical activity" (LRU-399-son). neolex.uz/en/laws/law-2856466/8 (lex.uz/docs/6819757)