The Advanced Certificate Course in Clinical Trials and Pharmacovigilance is a six-monthprogram. The course is divided into two phases: a three-month Theory Phase, conductedweekly to cover essential concepts such as clinical research processes, regulatory guidelines,trial operations, pharmacovigilance, and data management; and a three-month InternshipPhase that provides hands-on exposure in real-world settings like hospitals, clinical sites, andresearch organizations. Delivered by experienced professionals, the curriculum is designed tobridge the gap between academic learning and industry expectations, ensuring participants gainpractical insights into site monitoring, data collection, protocol development, and safetyreporting. The program also emphasizes career readiness through resume building, mockinterviews, and soft skills development, preparing students for roles such as Clinical ResearchAssociate (CRA), Clinical Research Coordinator (CRC), Pharmacovigilance Associate, andClinical Data Management (CDM) Executive. Graduates emerge with the expertise to navigatethe complexities of clinical trials and pharmacovigilance, making them valuable assets toresearch teams and healthcare projects focused on drug development and patient safety.