General Information on Applications
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.
Documents on national requirements
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