Master of Pharmacy (MPharm) in Pharmaceutical Regulatory Affairs

Overview

Pharmaceutical Regulatory Affairs (PRA) is a vital unit in a pharmaceutical company that successfully drives the Research & Development (R&D) efforts of the company to the market. The regulatory department works with a focus to get products to the market with a commercially viable label, in the least possible time and expense. The outcome of the program is to make available a pool of competent professionals in the area of Pharmaceutical Regulatory Affairs with fundamental knowledge on : Various Good Regulatory Practices in the Healthcare and related industries, Documentation and general principles involved in regulatory writing and submission to agencies ,Audit, inspections, Quality management system and Product Life Cycle Management, Clinical drug development and research regulations in India, EU and US, Regulations for Drugs, Cosmetics, Medical Devices, Herbals, Biologics, Food and Nutraceuticals in various countries like India, EU, US, Canada, Japan, ASEAN, etc.

Eligibility

A candidate who has passed B. Pharm degree examination from any recognized University and has secured not less than 55% of the maximum marks (aggregate)

Minimum Education