Registration of medicinal products
Frequently asked questions
“Armedika – provides services for registration of medicinal products, renewal of marketing rights and introduction of medicinal products into the markets in the Baltic States and Belarus.
- Registration of medicinal products (national, decentralised (DCP), mutual recognition (MRP)
procedures); - Renewal of the marketing authorisation for medicinal products;
- Periodic security reporting;
- Type IA, IB, II variations and other unrelated changes;
- Reclassification of medicinal products;
- Pharmacovigilance;
- Preparation of the package leaflet in accordance with the PCS and/or readability guidelines;
- A study on the consumer readability of the package leaflet.
For enquiries, please email: reg@armedika.lt
Services in Lithuania, Latvia, Estonia, Poland and other EU countries:
Contact person:Augusta Ževžikovienė
E-mail: augusta.zevzikoviene@armedika.lt;
Mob.tel.: +370 688 81118
Services in Belarus and Kazakhstan:
Contact person: Aras Tarabilda
E-mail: reg@armedika.lt