News

European Commission (EC) has published a new version of the Questions & Answers document on “Safety Features for Medicinal Products for Human Use (V.19)”.

The European Commission has taken decision to extend the transitional period for a period of three years, which was determined in the context of the action of the medicine verification system regarding the medicine products exported to the United Kingdom* (UK) following its’ withdrew from the European Union.

Welcome to the “EMVS Community Holiday Bulletin 2021”, a collaboration between the European Medicines Verification Organisation (EMVO) and the National Medicines Verification Organisations (NMVOs).

On November 22, 2021, a General Assembly of the Latvian Medicines Verification Organisation (LZVO) was held, where the strategy and budget for 2022 were approved, as well as a report on the most significant work done this year was presented.

In order for patients to receive only safe medicines, pharmacies and health care institutions in the first nine months of 2021 have checked in the verification system and handed over 19 million packages of medicines to residents in Latvia.

Inese Erdmane, Chairwoman of the Board at LZVO share insights of the Latvian medicine’s verification process with Dansk Medicin Verifikation Organisation Newsletter.