The followings are the list of Regulatory Authority for Pharmaceutical Industries.
FDA- Food and Drug Administration (USA)
TGA-Australian Government Department of Health and Therapeutic Goods Administration
MHRA- Medicines Healthcare Products Regulatory Agency (UK)
CDSCO- Central Drug Standard Control Organization (India)
HC- Health Canada
EPA- European Medicines Agency (Europe)
DMA- Danish Medicines Agency (Denmark)
MEDSAFE-New Zealand Medicines and Medical Device Safety Authority
LV-Medical Products Agency, Läkemedelsverket (Sweden)
PMPB - Pharmacy, Medicines, and Poisons Board (Malawi)
TFDA - Tanzania Food and Drug Authority
NAFDAC - National Agency for Food and Drug Administration and Control (Nigeria)
PPD - Pharmacy and Poisons Board (Kenya)
NDA - National Drug Authority (Uganda)
FDA - Food and Drug Administration (Philippines)
MOH - Ministry of Health (Kazakhstan)
MOH - Ministry of Health (Vietnam)
MOH - Ministry of Health (Cambodia)
MOH - Ministry of Health (Nepal)
FDA - Food and Drug Authority (Ghana)
DPML - Drug, Poisons, and Pharmacy Board (Ivory Coast)
MSP - Ministry of Public Health (Congo Brazzaville)
NMRA - National Medicines Regulatory Authority (Sri Lanka)
BDA - Medicines and Healthcare Products Regulatory Agency (MHRA) Europe
US-NSA - United States National Security Agency
FMHAC - Food, Medicine, and Healthcare Administration and Control Authority (Ethiopia)
NMPBA - National Medicines and Poisons Board Authority (Sudan)
MCA - Medicines Control Authority (Zimbabwe)
EU GMP - European Union Good Manufacturing Practice
Please note that there might be changes or
updates to these agencies, and you should verify the information based on the
most recent sources.
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