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 Medicines Verification System (CZMVS).
The End-user Registration Process necessary to connect to the national authentication system is described in the detailed instructions here.
Detailed Guide to CZMVS Portal here.
No charges/fees are required from distributors to be paid to NOOL.
NOOL offers a connection to the Alert Management System (AMS), where it is possible to quickly and conveniently resolve alerts via an API or web interface. More information about AMS functionalities can be found in the attachments below and on the "Alerts Management" section.
Emergency Verification Application (EVA)
Provides an interim solution for medicines verification in case the Czech Medicines Verification System (CZMVS) has problems or own verify aplication is not working. It can be accessed from any computer that has an attached keyboard, a supported web browser and internet connectivity. It does not support a scanner, and is not intended to be used as a permanent replacement for an integrated client system. Individuals wishing to use the EVA must already have approved user accounts set up via the CZMVS administration portal. Users must have sucessfully completed the registration process.
Recommendations for wholesalers whose medicines are contractually verified by a third party
Third-party verification options and specific solution instructions can be found among the documents listed below (Guide-Third-Party Verification).