Thursday, 5 September 2013

REGULATORY AGENCIES AND THEIR DIRECTORIES



North American Regulatory Agencies

USFDA, USA
Health Canada, Canada

European Regulatory Agencies

EMA, Europe

EDQM, Europe

MHRA, UK

AFSSAPS, France

BfArM, Germany

AGES, Austria

FAMHP, Belgium

NCDC, Albania

SCDMTE, Armenia








Danish Medicines Agency, Denmark

State Agency of Medicines, Estonia

FiMEA, Finland

GDNA, Georgia

National Organisation for Medicines, Greece

National Institute for Pharmacy, Hungary

Irish Medicines Board, Ireland

Ministry of Health, Israel

Italian Medicines Agency, Italy

Ministry of Health , Kazakhstan

Department of Drug supply and medical equipment, Kyrgyzstan

State agency of medicines, Latvia

LLV, Liechtenstein

State Medicines Control Agency, Lithuania

Ministry of Health, Luxembourg

Medicines Authority, Malta

MEB, Netherlands

NMA, Norway

The Office for Registration of Medicinal Products, MedicalDevices and Biocidal Products, Poland















Australian Regulatory Agencies 

TGA, Australia

MEDSAFE, New Zealand


Asian Regulatory Agencies 

CDSCO, India

PMDA, Japan

SFDA, China

Health science Authority, Singapore

FDA, Thailand

DCO, Pakistan

Ministry of Health, Sri Lanka

DGDA, Bangladesh

Department of Drug Administration, Nepal

NA-DFC, Indonesia

SFDA, Saudi Arabia

KFDA, Korea

Pharmaceutical Services, Ministry of Health, Malaysia

JFDA, Jordan


South American Regulatory Agencies

ANVISA, Brazil

COFEPRIS, Mexico

ANMAT, Argentina

ISPCH, Chile

PHABAHAMAS, Bahamas

INVIMA,Columbia

MINISTERIO DE SALUD, Costa Rica

CECMED, Cuba

DROGASYFARMACIAS, Dominician Republic

MSPAS, Guatemale

Ministry of Health, Jamaica

MSPBS, Paraguay

Ministry of Health, Trinidad and Tobago

DIGEMID, Peru

MSP, Uruguay

Salut, Andorra


African Regulatory Agencies

MCC, South Africa

ANDS, Algeria

MOH, Botswana

Ministry of Health, Burkina Faso











Ministry of health, Morocco

Ministry of Health, Rwanda


SOURCE: regulatoryone

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