by Dr. Yashashwini Reddy | Jun 26, 2025
🧪 Pharmacovigilance in Clinical Trials ✅ What Is It? Pharmacovigilance in clinical trials refers to the detection, assessment, reporting, and prevention of adverse events (AEs) or adverse drug reactions (ADRs) during the clinical development phase of...
by Dr. Yashashwini Reddy | Jun 26, 2025
Here is a comprehensive list and explanation of ICH Guidelines related to Pharmacovigilance, which aim to harmonize safety monitoring practices across regulatory regions: ✅ Core ICH Guidelines for Pharmacovigilance Code Title Focus Area E2A Clinical Safety Data...
