• Հայերեն
  • Русский
  • English
pharm.am
  • Home
  • About us
  • Main Functions
  • News and Announcements
  • Publications
  • Veterinary medicines
  • Contacts
  • Legislation
  • Assessments fees
  • Medicines Registration
  • Medicines Registration By EAEU Rulles
  • Import and export of medicines
  • Clinical trials
  • GMP compliance
  • GDP compliance
  • Market surveillance
  • Essential Medicines
  • Drug safety monitoring
  • The Procurements Process
  • International cooperation
  • OTHER
The list of Legal acts reletad to activities of Good Practice Inspection department in the Scientific Center of Drug and Medical Technology Expertise after academician Emil Gabrielyan
Order of Minister of Health of the Republic of Armenia N335-A of February 05, 2021 "On defining of new validity data of Good Manufacturing Practice certificates for manufactures in the Republic of Armenia"
  • Register
  • Guide to using "Database of registered medicines"
  • Drugs safety profile
  • ONLINE report about adverse effect of medicine

GMP compliance

  • Good Manufacturing Practice compliance for medicinal products
  • Legal basis for conducting inspections
  • The list of authorized manufacturers in the Republic of Armenia
  • The Good Manufacturing Practice assessment comliance during the marketing authorization
  • Legal acts regulating the Good Manufacturing Practice system in the Republic of Armenia
  • International documents related to medicines manufacturing
  • The Good Manufacturing Practice certificates issued by the Ministry of Health of the Republic of Armenia
  • Frequently Asked Questions

  • RSS
  • Facebook
  • Twitter
  • Home
  • About us
  • Main Functions
  • Committees and Councils
  • News and Announcements
  • Publications
  • Veterinary drugs
  • Contacts
  • SiteMap

Back to Top

© 2023 pharm.am