Pharmacovigilance
Master drug safety monitoring, adverse event reporting and signal detection processes.
Overview
The Pharmacovigilance program at TechPharma builds expertise in monitoring, detecting, assessing and preventing adverse effects of pharmaceutical products. Students learn ICSR processing, MedDRA coding, causality assessment, signal detection, aggregate reporting (PSUR/PBRER) and global regulatory safety requirements (FDA, EMA, CDSCO), preparing them for roles in pharma, CROs and drug safety database companies.
Eligibility
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences Graduates
- Freshers and working professionals
Course Duration
3 Months (Weekday & Weekend batches available)
Career Opportunities
- Drug Safety Associate
- Pharmacovigilance Associate
- ICSR Processing Executive
- Safety Data Entry Specialist
- Signal Management Associate
Training Features
- Live ICSR case processing practice
- MedDRA and WHO-DD coding training
- Exposure to Argus and ARISg safety databases
- Industry-recognized certification on completion
- Dedicated placement support
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