Regulatory Affairs

Regulatory affairs is a specialized postgraduate program that focuses on the regulations, guideline and compliant aspects for pharmaceutical industries. It deals with both national and international drug approval process like good manufacturing practices (GMP), Good laboratory practices (GLP) and good clinical practices (GCP). The field that bridges the gap between pharmaceutical companies and drug regularity authorities.

Drug regulatory affairs provide a pathway of students to become experts in the regulatory aspects of the Pharmaceutical Industry, ensuring the safe and effective development and marketing of Pharmaceutical Products.