General Information on Applications
e-SUBMISSION
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Guidance documents
Requirements on submissions for new marketing authorisation
Requirements on submissions for post-authorisation applications
National Authorities' fees, terms of payment and addresses
Guidance on national-specific labelling/package leaflet information
Recommendations on labelling and packaging of veterinary medicinal products
Publication of marketing authorisations
Product samples for visual/laboratory control by NCAs
Best Practice Guide for allocation of MRP/DCP procedure numbers
National fees
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Austria (AT - EN version), Belgium (BE), Bulgaria (BG), Croatia (HR), Cyprus (CY), Czech Republic (CZ, EN version), Denmark (DK), Estonia (EE, EN version), Finland (FI), France (FR), Germany - PEI (DE), Germany - BVL (DE), Greece (EL), Hungary (HU), Iceland (IS), Ireland (IE), Italy (IT, EN version), 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 NI).