Course Description
M. Pharm. in Drug Regulatory Affairs is spread over 4 semesters, and essentially aims to offer to eligible candidates advanced lessons in:
Regulatory and Quality Compliance in the pharmaceutical industry,
Pharmaceutical Regulatory Affairs, National and International Drug Approvals & Bio-ethics, Modern Analytical Techniques, Research Methodology & Pharmacological Screening, International Regulatory Systems, Clinical Trials & Healthcare Policies, National Regulatory Affairs,
Emerging Concept in Regulatory Affairs, Quality Assurance GLP,
GMP & Validation, Drug Regulatory Affairs.