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Welcome to EudraGMP

EudraGMP is a Community database containing information on all pharmaceutical manufacturers located in the EEA and other manufacturers which have been inspected by EEA national competent authorities (NCAs). It includes details of those manufacturers' Manufacturing and Importation Authorisations and GMP Certificates.

Read-only access to EudraGMP

Information in the EudraGMP database will be completed and updated on an ongoing basis. Only limited data from some EEA NCAs is available in this public version. Due to the timing of national inspections and the fact that the normal inspection cycle is about 3 years, as well as different approaches to technical implementation of the database at a national level, it is not expected that complete information will be available until 2011.

The table below lists all National Competent Authorities (NCA) of the EEA who have at this moment significant data in the EudraGMP database and have made information publicly available in EudraGMP, indicating the type of information that is provided.

CountryCompetent Authority AcronymEnglish NameScopeGMP ComplianceExpected GMP Publication DateManufacturing and Importation AuthorisationExpected MIA Publication DateURL
Belgium
BE_DGMP
Federal Agency for Medicines and Health Products
Human, Investigational Medicinal Product, Veterinary
2010-01-01
http://www.fagg-afmps.be/en/famhp
Bulgaria
BG_BDAV
National Veterinary Service Bulgaria
Bulgaria
BG_BDA
Bulgarian Drug Agency
Human, Investigational Medicinal Product
2011-12-01
Cyprus
CY_VS
Veterinary Services
Veterinary
Cyprus
CY_PSMOH
Pharmaceutical Services Ministry Of Health
Human, Investigational Medicinal Product
Czech Republic
CZ_USKVBL
Institute for State Control of Veterinary Biologicals and Medicaments
Veterinary
Czech Republic
CZ_SUKL
State Institute for Drug Control
Human, Investigational Medicinal Product
Denmark
DK_DKMA
Danish Medicines Agency
Human, Investigational Medicinal Product, Veterinary
2010-12-31
2009-10-01
http://www.laegemiddelstyrelsen.dk/hentmedie.asp?filID=7019
Estonia
EE_SAM
State Agency of Medicines
Human, Investigational Medicinal Product, Veterinary
Greece
GR_NOM
National Organization for Medicines
Human, Investigational Medicinal Product, Veterinary
2009-12-31
Hungary
HU_NIP
National Institute of Pharmacy
Human, Investigational Medicinal Product
Hungary
HU_IVMP
Central Agricultural Office, Directorate of Veterinary Medicinal Products
Veterinary
Iceland
IS_IMCA
Icelandic Medicines Control Agency
Human, Investigational Medicinal Product, Veterinary
Italy
IT_DGSAFV
Ministry for Labour, Health and Social Affairs - Department of Veterinary Public Health, the Nutrition and Foods Safety - Directorate General of Animal Health and Veterinary Medicinal Products - Office V-
Veterinary
2010-12-31
Latvia
LV_SAM
Latvian State Agency of Medicines
Human, Investigational Medicinal Product, Veterinary
2010-01-01
http://www.zva.gov.lv/index.php?id=442&lang=&top=112&sa=439
Lithuania
LT_SMCA
State Medicines Control Agency under the Ministry of Health of the Republic of Lithuania
Human, Investigational Medicinal Product
Malta
MT_MA
Medicines Authority
Human, Investigational Medicinal Product
Portugal
PT_INFARMED
National Authority of Medicines and Health Products, I.P.
Human, Investigational Medicinal Product
Romania
RO_NMA
National Medicines Agency
Human, Investigational Medicinal Product
Slovakia
SK_SIDC
State Institute for Drug Control
Human, Investigational Medicinal Product

Other NCAs will make the information available in the future. The above table will be updated accordingly.
 
 
     
 
 
 
The EudraGMP database is maintained and operated by the EMEA. Access to the general public is granted in order to enhance availability of information related to the EMEA mandate. The content of the database is provided by the National Competent Authorities (NCA) of the EEA. For this reason, the EMEA accepts no responsibility or liability whatsoever (including but not limited to any direct or consequential loss or damage it might occur to you and/or any other third party) arising out of or in connection with the information on this database. Any questions about the content should be addressed to the relevant NCA. Please click here to get list of NCA's.
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