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Marketing authorisation of veterinary medicinal products

The marketing authorisation applications should be submitted in accordance with the Veterinary Medicinal Products Regulation (Regulation (EU) 2019/6).

Regulation (EU) 2019/6


Procedural guidance on decentralised, mutual recognition and subsequent recognition procedures is provided by CMDv.

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

For veterinary medicinal products a filled out request form available on the CMDv website should be provided.

Application forms and information on fees

The use of the eAF (electronic application form) will be mandatory from 1st January 2016 for all applications (human and veterinary MRP, DCP and national procedure applications for marketing authorisation, renewal and variations). Further details can be found on: eSubmission: VET eSub ( and CMDv website.


There are two types of fees for the marketing authorisation applications in Estonia.

The state fee has to be paid prior the submission of the application. For the assessment fees, the invoice will be issued upon receipt of the valid application. No payment of assessment fee should be made in advance.

You can find all State and Assessment fees here.

Last updated: 04.11.2022