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You are here: Home / News / The Federal Antimonopoly Service has prepared another version of the document on compulsory licensing of pharmaceuticals

The Federal Antimonopoly Service has prepared another version of the document on compulsory licensing of pharmaceuticals

The latest version of the document that defines the FAS’s position on compulsory licensing of medicines has become available to Pharmvestnik. No version of the draft legislation has yet appeared on the regulation.gov.ru site.

http://regprof.org/viewtopic.php?f=6&t=876&p=3855&sid=ee0332dfe32ad00fa68c25cf7d253d7b#p3855

19.09.201610.10.20160
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  • About
    • Our experts
    • Feedback
    • Our news
      • Russian/EEU GMP
    • Charity
  • Services
    • Fast registration of medical devices according to the Decree # 430
    • Registration of pharmaceutical products (PP). Registration of pharmaceutical substances
    • Medical devices marketing registration
    • Clinical studies of pharmaceutical products
    • Registration of biologically active additives
    • Registration of veterinary pharmaceutical products and feed additives
    • Registration of infant and specialized food.
    • Registration of perfume and cosmetic products and oral hygiene products
    • Declaration and certification
    • Registration of mineral water
    • Customs support
    • Registration of trademarks and intellectual property
    • Market Research
    • Authorized representative function
    • Russian/EEU GMP
  • Clients
  • Articles
    • Registration (marketing authorization) of drugs in Russia
    • Eurasian Economic Union. Single market for medical products
    • Registration of medical devices in Russia
    • Clinical trials in Russia
    • Audit of manufacturing sites. Russian GMP certificate
    • Registration of dietary supplements in Russia
  • Request
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