On 18 May 2017 the general meeting of Mana Aptieka was held, where Inese Erdmane, the Executive Director of the Latvian Medicines Verification Organisation, presented the Falsified Medicines Directive and Delegated Regulation, which came into force on 9 February 2016.
Regulation on mandatory safety features for medicines refer to medicines for humans, and in relation to the fact on how to prevent from getting of falsified medicines into the legal supply chain. At the end I.Erdmane introduced the audience with the Latvia Medicines Verification Organisation, purposes and tasks thereof as well as the course of introduction of the medicines verification system in Latvia.