M.Pharm in Pharmaceutical Regulatory Affairs is a specialized program designed for students aiming to pursue a career in the regulatory aspect of the pharmaceutical industry. This course typically lasts 2 years and provides in-depth knowledge of regulatory requirements, guidelines, and legal frameworks in the global pharmaceutical market. Students will explore topics such as drug development processes, regulatory compliance, quality assurance, and the role of regulatory agencies. The program equips students with the skills necessary to navigate the complexities of regulatory affairs, ensuring that pharmaceutical products meet safety, efficacy, and quality standards. Graduates can work in pharmaceutical companies, government agencies, consultancy firms, and international health organizations, contributing to the safe distribution of pharmaceutical products worldwide.
