Post Marketing Surveillance – Medical Devices and In Vitro Diagnostics

Manufacturers are reminded to submit biennial PMS report of the respective device including any adverse events as per requirement of the Tanzania Medicines and Medical Devices (Control of Medical Devices) Regulations, 2015

  • Evaluation Report on Post Marketing Surveillance Programme for Medical Devices and In Vitro Diagnostics (2020/21 - 2022/23), May, 2024 Download