News

On 13 January 2021, the European Commission adopted a new Delegated Regulation, amending Delegated Regulation (EU) 2016/161 as regards a derogation from the obligation of wholesalers to decommission the unique identifier of products exported to the United Kingdom.

The Latvian medicines verification system, which was established in Latvia to check the safety of medicines and prevent people from receiving or buying falsified medicines, has been fully operational for almost two years.

European Medicines Verification Organisation (EMVO) was published frequently asked questions regarding verification system and Brexit.

Attesting their qualification and high operating standards of the LZVO, more and more specialists of the Latvian Medicines Verification Organisation (LZVO) hold positions at the international level.

EMVO has been working to manage the implications of Brexit (the UK’s departure from the EU Internal Market rules) for the EMVS and its users.

A new version of the European Commission’s Questions & Answers document on “Safety Features for Medicinal Products for Human Use (V.18)” is available from August 11.