About this document
The Guidelines on Regulatory Reliance for Marketing Authorisation of Human Medicinal Products July, 2025 was issued by the Tanzania Medicines and Medical Devices Authority (TMDA), which regulates medicines, medical devices and diagnostics. It is dated 2025. The full text is available above as a PDF (1 MB), free to read and download.
This document is reproduced as published by the issuing authority. For advice on how it applies to your circumstances, speak to our team.