LEARN ABOUT
Pharmacovigilance
Mandate
Department of Pharmacovigilance and Clinical Trials at BoMRA is responsible for the following functions:
- Pharmacovigilance - Safety monitoring of human medicines, vaccines, veterinary medicines, and medical devices.
- Oversight and Regulation of Clinical Trials
- Post Marketing Surveillance of medical products for quality defects including Substandard and Falsified Medicines.
Organogram
- CEOHead of Department
- MainSupervisor
- MidStaff
- MidStaff
- MidStaff
- MainSupervisor
- MidStaff
- MidStaff
- MidStaff
To achieve its mandate and objective the Directorate/Department works very closely with different stakeholders including;
- Public Health Programmes
- District Health Management Teams
- Professional bodies
- Academia
- Healthcare professionals
- Healthcare Facilities
- Market Authorisation Holders
- Research Institutions
- Patients
Below is a graphical presentation of the stakeholders and how each fits into the medicines/vaccine’s safety surveillance activities.