The Master of Pharmacy (M.Pharm) in Drug Regulatory Affairs is a comprehensive program that provides advanced knowledge in regulatory policies, drug development, and quality management. The curriculum covers key areas such as regulatory guidelines, pharmaceutical laws, intellectual property rights, clinical trials, and pharmacovigilance.
Students gain expertise in the preparation of regulatory documents, submission of drug applications, and adherence to regulatory frameworks set by organizations like the FDA, EMA, and CDSCO. The program also emphasizes ethical practices, quality assurance, and risk management, preparing graduates for pivotal roles in regulatory affairs departments of pharmaceutical companies, research organizations, and government agencies.
Graduates can pursue careers as Regulatory Affairs Officers, Drug Safety Associates, Quality Assurance Managers, or work in clinical research, drug licensing, and policy development.
.jfif)
.jfif)