Distributors/wholesalers of pharmaceutical products in the Czech Republic will be required to verify prescription-only medicine packs according to the EU Directive 2011/62/EU - also called the Falsified Medicines Directive (FMD) in specific circumstances.
Wholesalers in the Czech Republic will have to adapt their software systems to create a connection to Czech National Medicnes Verification System (CZNMVS).
An on-boarding process with NOOL necessary for connecting the subject to NMVS will be described below. Subjects not participating in the pilot can start registration within October 2018. Companies that have not received a registration letter for a variety of reasons should contact us at email@example.com as soon as possible.
The End-user Registration Process necessary to connect to the national authentication system is described in the detailed instructions here.