TMDA operates Tanzania's national pharmacovigilance and medicine-safety reporting system.
Core official resources
- Reporting ADRs and AEFIs — current reporting mechanisms and forms.
- Electronic submission — online reporting information.
- TMDA — authority portal, safety information and registered-product resources.
Important national distinction
TMDA currently supports several national reporting routes: web-based SQRT, mobile application, USSD and paper reporting. The authority states that all suspected adverse events should be reported, whether serious or non-serious and whether known or unknown.