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TMDA is responsible for regulating safety, quality and effectiveness of medicines, medical devices and diagnostics. TMDA main responsibility is stated in the Health policy, 2007 and its mandate is stipulated in the Tanzania food, drugs and cosmetics act (TFDCA) cap. 219 as amended by the Finance Act of 2019.
The act provides for the efficient and comprehensive Regulation and control of safety and quality of medicines, medical devices and diagnostics in Tanzania mainland. In order to improve public service delivery, TMDA is managed as an Executive Agency in accordance with the Executive Agencies Act, cap.245 as amended in 2009.
We can help you with your TMDA registration. Tanzania Medicines and Medical Devices Authority (TMDA) is responsible for protecting and promoting public health by ensuring:
CATEGORIES OF TMDA REGULATED INVESTMENTS ARE THE MANUFACTURERS AND DEALERS OF:
Any person who is dealing with manufacturing, importation and distribution of Medicines, medical devices, laboratory equipment and diagnostics.