Pharmacovigilance activities in Tanzania Mainland-The Role of TMDA_with Jonah comments

This presentation describes the regulatory framework, pharmacovigilance (PV) activities, and safety monitoring system in Tanzania, focusing on TMDA’s mandate to ensure that medicines, vaccines, medical devices, and diagnostics are safe, effective, and of good quality. It highlights both passive and active surveillance systems, the process of adverse event following immunization (AEFI) investigations, and TMDA’s achievements and challenges.