M.Pharma in Drug Regulatory Affairs is a specialized postgraduate degree that normally lasts 2 years. It focuses on the regulatory aspects of pharmaceutical products, such as drug development, approval processes, and compliance with national and international standards. The curriculum includes topics like pharmaceutical legislation, regulatory writing, clinical research, pharmacovigilance, and quality assurance. Graduated acquire experience writing regulatory submissions, comprehending worldwide regulatory standards, and managing product lifecycles. Students get the career opportunities to work in pharmaceutical businesses, regulatory agencies, and consulting organizations, where they play critical roles in assuring drug safety, efficacy, and regulatory compliance.
