By the Resolution of the Government of the Russian Federation from June 30, 2004 № 323 “On Approval of Provision on the Federal Service for Surveillance in Healthcare” (paragraph 5.1.4.2) Roszdravnadzor is vested the powers to perform federal state supervision over circulation of medicines by means of inspections of medicines for compliance with compulsory requirements set to their quality.
The section “Regulatory Documents” (Нормативные акты - Russian version of the web-site) contains: regulatory acts, which specify requirements for medicines throughout their circulation (supervision over quality of medicines during their manufacture, storage and sale); information letters of Roszdravnadzor, listing of medicines subject to withdrawal; information and analytical materials on the results of inspections by Roszdravnadzor.
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