MSc Drug Development & Regulatory Affairs

🎓 Postgraduate · Pharmaceutical & Regulatory Sciences

Course Overview

The MSc in Drug Development & Regulatory Affairs focuses on how medicines are researched, tested, approved, and regulated before reaching patients.

Students learn about clinical trials, regulatory guidelines, and compliance requirements followed by global pharmaceutical companies. This program is ideal for students seeking non-clinical roles in the pharmaceutical and healthcare industries.

Key Program Highlights

  • Strong focus on drug approval and regulations
  • Industry-oriented curriculum
  • High relevance in global pharma and biotech sectors

Popular Specializations

  • Regulatory Affairs
  • Clinical Trial Management
  • Drug Safety & Compliance

Career Opportunities

  • Regulatory Affairs Executive
  • Clinical Trial Coordinator
  • Drug Safety Associate
  • Pharmaceutical Compliance Officer

Requirements

Academic Requirements
  • Bachelor’s degree in Pharmacy / Life Sciences / Chemistry
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₹ 20L - ₹ 28L
Tuition fee
Disclaimer: Fees are indicative and subject to change.
Intake September
Duration 1–2 years
Mode of study Full Time
Fees and deadlines depend on the selected options. Fees and currency conversion are approximate.