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Guidelines for Pharmaceutical Manufacturers/Marketing Authorisation Holders on Managing Alerts Generated in the Verification and Decommissioning of Medicinal Products in the BgMVS
02 March 2021
Letter to stakeholders regarding the implementation of safety features under the Falsified Medicines Directive 2011/62/EU
Data Matrix – A solution to counterfeiting of medicines and in the service of traceability
EMA Implementation Plan
EMVO on-boarding / NMVO contracting
European Pack Coding Guideline, version 4.0, July 2017
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Home
The initiative
Who are we
Members
Partners
Statute
Financial report
Contacts
Users of the system
Manufacturers
MAHs
Parallel importers
Wholesalers
Pharmacies
IT Providers
Legal acts
Presentations
Other documents
Frequently asked questions
News and events
