The final meeting of the Russian Ministry of Industry and Trade Collegium took place on May 27, attended by deputy prime ministers and representatives of...
Three-year transitional period for GMP certification
The Association of International Pharmaceutical Manufacturers (AIPM) proposes introducing a three-year transitional period for pharmaceutical companies, during which importers will be able to present Good...
Roszdravnadzor regulation developed for the registration of maximum sale prices for implantable medical devices
The Russian Health Ministry has developed a draft departmental order: «On approval of the Administrative Regulation of the Federal Service for Surveillance in Health Care...
Amendments to the Federal Act “On the circulation of pharmaceutical products”
The Federal Act was adopted by the State Duma on June 30, 2015 and approved by the Federation Council on July 8, 2015. «In order...
Rules for registration and expert examination of medicines have been developed for EEU.
The Working Group of the Eurasian Economic Commission for the formation of common approaches to the regulation of the circulation of pharmaceutical products in the...