• Marketing authorisations (registration)
  • Medicinal products authorised in Estonia
  • Granting marketing authorisations
• Drug information
• Clinical trials
• European Pharmacopoeia
• Classification of medicinal products
• Pharmacovigilance and Adverse Drug Reactions
• Manufacture of Medicinal Products
• Pharmacy regulations
• Wholesale of Medicinal Products
• Drug statistics

Decentralised procedures with Estonia as RMS  

12 February 10

The companies wishing to use Estonia as the Reference Member State are advised to contact the State Agency of Medicines well in advance.

The requests for DCP with Estonia as a RMS should be sent to mrp@ravimiamet.ee.

For request, please fill in the request form published on the CMDh web-page.

The applicants will be informed whether a time slot has been booked for their submission or not.

SAM should be notified of any changes in agreed submission dates. The changes in active ingredients are decided on a case-by-case basis.

The next slots for decentralised procedures are available for 2012 Q3-Q4.