Pharmacovigilance & Regulatory Affairs Workshop

The Pharmacovigilance & Regulatory Affairs Workshop was organized by Guru Nanak College of Pharmaceutical Sciences to enhance students’ knowledge of drug safety monitoring and regulatory compliance in the pharmaceutical sector. The workshop focused on developing essential skills such as adverse drug reaction (ADR) reporting, safety data analysis, regulatory documentation, risk assessment, and understanding national and international regulatory guidelines. Eminent industry experts and regulatory professionals shared practical insights and real-world experiences to guide students on pharmacovigilance processes, post-marketing surveillance, and regulatory submissions. Interactive sessions, case discussions, and hands-on activities strengthened participants’ analytical abilities and professional competence. The program successfully encouraged students to understand their responsibility in ensuring drug safety, maintaining regulatory standards, and contributing to public health.