M PHARM - DRUG REGULATORY AFFAIRS

M Pharm in Drug Regulatory Affairs is a postgraduate program that focuses on providing advanced education and training in the field of drug regulatory affairs. The course is designed to provide students with a comprehensive understanding of pharmaceutical regulations and compliance, as well as the skills needed to navigate the complex and ever-evolving regulatory landscape in the pharmaceutical industry.

Course Highlights

Understanding the national and international regulatory frameworks governing the pharmaceutical industry.
Knowledge of the procedures and documentation required for the registration and approval of pharmaceutical products.
Ensuring compliance with regulatory standards and implementing quality assurance practices in drug development and manufacturing.
Studying the monitoring and reporting of adverse drug reactions and ensuring compliance with safety regulations.
Understanding ethical considerations and legal aspects related to drug development and marketing.

Career Scope

M Pharm in Drug Regulatory Affairs offers a diverse range of career opportunities for graduates in the pharmaceutical and regulatory sectors. Here are some potential career scopes for individuals with an M Pharm in Drug Regulatory Affairs:

Regulatory Affairs Specialist
Regulatory Affairs Manager
Quality Assurance Specialist
Pharmacovigilance Specialist
Regulatory Compliance Officer
Drug Safety Officer
Clinical Research Regulatory Coordinator

Program Overview

Duration : 2 Years
Eligibility : Pass in 10+2 / ‘A’ Level or its equivalent from any Board or Council with 45% aggregate marks in Physics, Chemistry, Mathematics and Biology / Zoology / Computer Science.

Course Content