M.Pharma in Executive Drug Regulatory Affairs is a 2-year postgraduate program designed for professionals seeking expertise in the regulatory aspects of pharmaceuticals. The course focuses on drug development, registration, regulatory compliance, and market authorization processes in both national and international settings. Students acquire an in-depth understanding of drug laws, quality control, clinical trials, and pharmacovigilance, alongside skills in navigating the regulatory requirements of different regions such as the FDA, EMA, and other global bodies. The program combines theoretical knowledge with practical experience, often through case studies, internships, and projects. Graduates are equipped to work in the pharmaceutical industry, regulatory agencies, and consultancy firms, handling drug approvals, policy development, and ensuring compliance with global pharmaceutical regulations.
