Drug Safety & Efficacy
Regulatory → Assessment → Insights
- Fundamentals of pharmacovigilance and its role in healthcare
- Adverse event detection, reporting, and signal management
- Regulatory standards and global guidelines (ICH, FDA, EMA)
- Risk assessment and benefit‑risk analysis
- Safety data interpretation and decision‑making
- Real‑world case studies from pharmacovigilance practice
- Full access to all recorded modules
- Practical workflows and case‑based understanding
- Certificate of completion (if included in product package)









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