To provide the students with the basic concepts, adverse drug reactions reporting system and tools used in Pharmacovigilance to improve public health in relation to the use of medical interventions.
Topics Covered
Module I – Basic Concepts in Pharmacovigilance
Module II – Pharmacovigilance Methods
Module III – Adverse Event Reporting System in PV
Module IV – Case Processing
Module V – Pharmacovigilance Database and Signal Identification
Module VI – Risk Assessments, Evaluation & Management in PV
Module VII – Laws & Regulatory Guidelines in PV
Module VIII – medDRA
Eligibility
Bachelor’s, Master s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) / B.Sc./M.Sc, M.Pharmacy, M.Sc /MA (Statistics) and all professionals working with Pharmaceutical companies, CROs and Hospitals.