On 14 September the meeting for introduction of the Latvian Medicines Verification System will take place

The meeting is organised by the Latvian Medicines Verification Organisation in cooperation with the IT partner Arvato Systems. The seminar will take place in the conference centre of the hotel Radisson Blue Latvija, at Elizabetes iela 55, Riga.

In February 2016 the Falsified Medicines Directive and the European Commission Delegated Regulation came into force, the purpose of which is to protect patients from acquisition of falsified medicines through legal supply chain, as well as to ensure operation of the local market of medicines in all countries of the European Union and the European Economic Area. The requirements of the Delegated Regulation will refer to medicines subject to prescription and medicines not subject to prescription – omeprazole, the packaging of which will contain unique safety features.

All representatives of producers, the medicines of which are subject to the requirements of the Falsified Medicines Directive, as well as representatives of pharmaceutical wholesalers, pharmacies, hospitals and other health institutions, who are responsible for the affairs of introduction of the Delegated Regulation in the particular health care institution, are invited to participate in Part 1 of the Seminar.

Suppliers/ providers of IT systems for pharmaceutical wholesalers and pharmacies, IT software for hospitals and other health institutions only will participate in Part 2 of the Seminar.

Number of seats is limited! Participation in the seminar: free of charge. Working languages: Latvian and English (without translation).

Please, apply your participation by 8 September (including), e-mail, specifying the name, surname, position held of the participant, name of the institution, e-mail and telephone number for communication.