This is for self-screening of the documentation in support of the registration of Medicines. It should be signed and stamped by the Marketing Authorization Holder
This is simplified guidance for the documentation for the registration of Medicinal products, for main content visit the compendium guidelines available at TMDA through https://www.tmda.go.tz/publications/42
This is summarized requirement for the documentation for registration of Class B, C, and D medical devices.
This is summarized requirement for the documentation for registration of Class B, C, and D medical IVDDs
