General Information on Applications
e-SUBMISSION
Please open the link above for further information
Documents relating to the former Chapter 7 of the Notice to Applicants provided by the European Commission
The information regarding veterinary medicinal products authorised nationally (Mutual Recognition Procedure/Decentralised Procedure) contained in Chapter 7 - General Information of the Notice to applicants - had been transferred to the CMDv website respectively.
Format and no. of copies post-authorisation procedures
updated February 2019
Payment terms & addresses for national fees
updated November 2018
Packaging 'blue-box' requirements in NP/MRP/DCP/CP updated December 2018
Further information
National databases of authorised veterinary medicinal products
updated September 2018
Overview of MSs' requirements during national phase
updated March 2018
National fees
Please inform the CMDv secretariat if you find a link that does not work
Austria (AT - EN version), Belgium (BE), Bulgaria (BG), Croatia (HR), Cyprus (CY), Czeck Republic (CZ - EN version), Denmark (DK), Estonia (EE), Finland (FI), France (FR), Germany - PEI (DE), Germany - BVL (DE), Greece (EL), Hungary (HU), Iceland (IS), Ireland (IE), Italy (IT), Latvia (LV), Liechtenstein (LI - No fees regarding DCP/MRP applications due to an agreement between LI and AT. This agreement allows LI to accept marketing authorisations issued by the Austrian authority (AGES) for the MRP/DCP procedures, provided the applicant wishes to have LI included), Lithuania (LT), Luxembourg (LU), Malta (MT), Netherlands (NL), Norway (NO), Poland (PL), Portugal (PT), Romania (RO), Slovakia (SK), Slovenia (SI), Spain (ES), Sweden (SE), United Kingdom (UK)https://english.cbg-meb.nl/topics/bd-fees-and-product-types