Category

National agencies for drug regulation

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United States Food and Drug Administration

agency of the US Department of Health and Human Services

European Medicines Agency

highest regulatory authority on medicines in the European Union

Ministry of Health, Labour and Welfare

ministry of Japan

regulation of therapeutic goods

regulation designed mainly to protect the health and safety of the population, aiming at ensuring the safety, quality, and efficacy of the therapeutic goods

National Institute for Health and Care Excellence

non-departmental public body of the Department of Health in the United Kingdom

Medicines and Healthcare products Regulatory Agency

Medicine regulation agency in the UK

Brazilian Health Regulatory Agency

Brazilian government agency

Central Drugs Standard Control Organization

Apex Drug Regulatory Body

National Medical Products Administration

Chinese government agency

Indonesian Food and Drug Authority

Indonesian government agency

Institute for Quality and Efficiency in Health Care

German foundation in the healthcare sector

Pharmaceuticals and Medical Devices Agency

administrative agency in Japan

thumb|Logo of Swissmedic The Swiss Agency for Therapeutic Products (Swissmedic) is the Swiss surveillance authority for medicines and medical devices, registered in Bern. It began operations on 1 January 2002 as successor of (IKS), which was itself the successor of (SANZ). Swissmedic is affiliated to the Federal Department of Home Affairs.

EudraLex is the collection of rules and regulations governing medicinal products in the European Union.

Swedish Medical Products Agency

Swedish administrative authority

National Agency for the Safety of Medicine and Health Products

French public establishment for health risks

Therapeutic Goods Administration

regulatory body for therapeutic goods (including medicines, medical devices, gene technology, and blood products) in Australia

Finnish Medicines Agency Fimea

The Finnish Medicines Agency (Fimea; ) is a central agency under the Ministry of Social Affairs and Health that regulates medicines, medical devices, blood and tissue products, biobanks, and develops the pharmaceutical industry. Fimea was established in 2009, succeeding the National Agency for Medicines. Its predecessor, the National Agency for Medicines, had been operational since 1994.

Italian Medicines Agency

government organization in Rome, Italy

National Administration of Traditional Chinese Medicine

Chinese national administration

EudraVigilance (European Union Drug Regulating Authorities Pharmacovigilance) is the European data processing network and management system for reporting and evaluation of suspected adverse reactions to medicines or devices which have received marketing authorisation or are actively being studied in clinical trials in the European Economic Area (EEA). The European Medicines Agency (EMA) operates the system on behalf of the European Union (EU) medicines regulatory network.