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Regulations in the pharmaceutical field

The Ministry of Labor, Health and Social Protection of IDPs from the Occupied Territories of Georgia is responsible for regulating and supervising the pharmaceutical sector in Georgia, through the Agency for the Regulation of Medical and Pharmaceutical Activities.

For information about the production and sale of pharmaceutical products, visit the link

"The rules governing medicinal products in the European Union" contains guidance for the interpretation of the principles and guidelines of good manufacturing practices for medicinal products for human and veterinary use laid down in Commission Directives 91/356/EEC, as amended by Directive 2003/94/EC, and 91/412/EEC respectively.

For more information about GMP (Good Manufacturing Practice) and GDP (Good Distribution Practice) visit the link

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This document has been produced without formal United Nations editing. The designations employed and the presentation of the material in this document do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations Industrial Development Organization (UNIDO) concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries, or its economic system or degree of development. Designations such as “developed”, “industrialized” or “developing” are intended for statistical convenience and do not necessarily express a judgement about the stage reached by a particular country or area in the development process. Mention of firm names or commercial products does not constitute an endorsement by UNIDO.