Master of Pharmacy (M.Pharm) in Pharmaceutical Regulatory Affairs

Overview

Regulatory affairs (medical affairs) professionals (aka regulatory professionals) usually have responsibility for the following general areas:

• Ensuring that their companies comply with all of the regulations and laws pertaining to their business.
• Working with federal, state, and local regulatory agencies and personnel on specific issues affecting their business. i.e. working with such agencies as the Food and Drug Administration or European Medicines Agency (Pharmceuticals and medical devices); The Department of Energy or the Securities and Exchange Commission (banking).
• Advising their companies on the regulatory aspects and climate that would affect proposed activities. i.e. describing the "regulatory climate" around issues such as the promotion of prescription drugs and Sarbanes-Oxley compliance.

Eligibility

The candidate who has passed Bachelor's Degree in Pharmacy. Obtained at least 55% marks (50% marks in case of candidates belonging to reserved category) in the qualifying Examination.

Minimum Education