News

The Baltic meeting took place in Vilnius

24.04.2019.

The meeting of the Baltic States medicines agencies took place on 11th of April 2019 in Vilnius, Lithuania. Representatives of Lithuanian, Latvian and Estonian medicines agencies, both human and veterinary medicines, and...

BREXIT: regarding performance of pharmacovigilance responsibilities

12.03.2019.

The State Agency of Medicines would like to draw your attention to the following requirements regarding the Qualified person responsible for pharmacovigilance (QPPV) and Pharmacovigilance system master file (PSMF)...

Notice to stakeholders on the withdrawal of the United Kingdom and EU rules for national authorised medicinal products for human use

07.03.2019.

The United Kingdom submitted on 29 March 2017 the notification of its intention to withdraw from the Union pursuant to Article 50 of the Treaty on European Union. This means that as from 30 March 2019, 00:00h (CET (‘the...

News

The Baltic meeting took place in Vilnius

BREXIT: regarding performance of pharmacovigilance responsibilities

Notice to stakeholders on the withdrawal of the United Kingdom and EU rules for national authorised medicinal products for human use

Information on submissions of marketing authorisation documentation in eCTD format

Type IA/IAIN submission checklist for nationally authorized medicinal products

24th September 2018: Public Holiday

Welcome to our new website!

On the declaration of the prices of medicinal products

Changes in office hours of the State Agency of Medicines