Pharmacovigilance and Clinical Trials
Responsibilities
1. Ensure the safety and efficacy of products to protect public and animal health.
2. Adverse Drug Reactions (ADRs) and Vaccine-Related Events.
3. Scope: Monitoring ADRs and vaccine-related adverse events.
4. Ensure the safety and efficacy of medicines and vaccines used in humans.
5. Medical Devices - Surveillance of incidents related to medical devices.
6. Objective -Identify potential risks and ensure safety in healthcare settings.
7. Cosmetics -Focus: Monitoring adverse effects of cosmetic products.
8. Adverse events Reporting- Collecting and analyzing reports from healthcare professionals, manufacturers, and the public.
9. Evaluating risks associated with medicines, vaccines, medical devices, cosmetics, and veterinary products.
10. Implementing safety measures such as product recalls, label changes, or public warnings.
11. Stakeholder awareness.