This course introduces the principles and practices of pharmacovigilance with a focus on drug safety and adverse drug reaction monitoring. Students learn key concepts such as ADR reporting, causality assessment, post-marketing surveillance, and risk–benefit analysis. The course integrates theory with practical training in safety data evaluation and regulatory documentation. It prepares graduates for roles in drug safety, regulatory affairs, and patient-centric healthcare.
- Teacher: Dr. Prashant Prakash Shivgunde STPBL