Regional
- European Medicines Agency (EMA)
- For Inspections: Compliance - European Medicines Agency
- European Heads of Medicines Agencies
- For Human Medicines: Scientific guidelines - European Medicines Agency
- For Vet Medicines: Quality guidelines introduction - European Medicines Agency
- European Directorate for the Quality of Medicines & Healthcare
- European Commission: Medicinal products for human use
National Competent Authorities
- Austria: Austrian Medicines and Medical Devices Agency - Austrian Federal Office for Safety in Health Care
- Belgium: Federal agency for medicines and health products (FAMHP)
- Bulgaria: Bulgarian Drug Agency
- Croatia: Agency for Medicinal Products and Medical Devices (HALMED)
- Czech Republic: State Institute for Drug Control
- Denmark: Danish Health and Medicines Authority
- Estonia: State Agency of Medicines
- Finland: Finnish Medicines Agency
- France: French National Agency for Medicines and Health Products Safety (ANSM)
- Germany: Federal Institute for Drugs and Medical Devices (BfArM)
- Greece: National Organization for Medicines
- Hungary: National Institute of Pharmacy
- Iceland: Icelandic Medicines Agency
- Ireland: Health Products Regulatory Authority (HPRA)
- Italy: Italian Medicines Agency
- Latvia: State Agency of Medicines
- Liechtenstein: Office of Health/Medicinal Products Control Agency
- Lithuania: State Medicines Control Agency
- Luxembourg: Ministry of Health
- Malta: Medicines Authority
- Netherlands: Medicines Evaluation Board
- Norway: The Norwegian Medicines Agency
- Poland: Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
- Portugal: National Authority of Medicines and Health Products, IP (INFARMED)
- Romania: National Agency for Medicines and Medical Devices
- Slovakia: State Institute for Drug Control (SIDC)
- Slovenia: Agency for Medicinal Products and Medical Devices (ARSZMP)
- Spain: Spanish Agency of Medicines and Medical Devices (AEMPS)
- Sweden: Medical Products Agency (MPA)
- UK: Medicines and Healthcare Product Regulatory Agency (MHRA)
- UK: Veterinary Medicines Directorate - GOV.UK
Other National Authorities in Europe
- Andorra: The Ministry of Health and Welfare
- Georgia: Georgia Drug and Narcotics Agency
- Moldova: Medicines Agency
- Russian Federation: Federal Service on Surveillance in Healthcare and Social Development
- Serbia: Medicines and Medical Devices of Serbia
- Turkey: Turkish Medicines and Medical Devices Agency
- Ukraine: Ministry of Health
International Regulatory, Standards, and Harmonization Organizations
- International Conference on Harmonisation (ICH)
- International Medical Device Regulators Forum
- International Organization for Standardization (ISO)
- Organisation for Economic Co-operation and Development (OECD): Good Laboratory Practice (GLP)
- Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S)
- United Nations - Global Issues Health
- World Health Organization (WHO)
- World Intellectual Property Organization (WIPO)