The Food and Drugs Authority will continually ensure quality, safe and efficacious / effective / wholesome products through Registration, Inspections, Licensing, Surveillance and Clinical Trials activities in conformity with the applicable national and international standards and to meet customer satisfaction. The Food Drugs Authority (FDA) is the National Regulatory Body responsible for the Pharmaceutical regulation of food, Pharmaceutical drugs, food supplements,Nutraceutical products, herbal and homeopathic medicines, veterinary medicines,Feed Supplements, cosmetics, medical devices, household chemical substances, tobacco and tobacco products and the conduct of clinical trials protocols.
The FDA has four (4) technical advisory committees (TAC) for safety of medicines, safety of vaccines and biological products, medical devices and clinical trials. The committees are made up of experts from different scientific backgrounds. The TAC on safety was formed to act as a forum to advise the FDA on matters relating to post-approval safety, efficacy, and effectiveness of the products granted marketing authorization by the Authority. The TAC for clinical trials also advises the FDA on matters related to the conduct of clinical trials. The TAC provides expertise to assist the FDA in making appropriate risk management decisions, however, the decision making responsibility remains with the FDA.
The FDA has four (4) technical advisory committees (TAC) for safety of medicines, safety of vaccines and biological products, medical devices and clinical trials. The committees are made up of experts from different scientific backgrounds. The TAC on safety was formed to act as a forum to advise the FDA on matters relating to post-approval safety, efficacy, and effectiveness of the products granted marketing authorization by the Authority. The TAC for clinical trials also advises the FDA on matters related to the conduct of clinical trials. The TAC provides expertise to assist the FDA in making appropriate risk management decisions, however, the decision making responsibility remains with the FDA.
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