M.S. in Drug Regulatory Affairs

M.S. in Drug Regulatory Affairs

Long Island University

New York, New York, USA
M.S. in Drug Regulatory Affairs
Duration1.5-2 Years
LevelMasters Program
  • The mission of the Master of Science program in Drug Regulatory Affairs is to prepare students to become lifelong learners and leaders in a variety of settings including biotechnology, medical devices, pharmaceuticals, consulting arena, and liaise with government and regulatory agencies worldwide
  • Students will study courses like Biostatistics, Drug Regulatory Affairs, Pharmaceutical Labeling, Advertising, and Promotion, FDA Regulation of Over-the-Counter Drugs, Medical Devices and Dietary Supplements, Principles and Practices of Regulatory Compliance and Enforcement, Mechanics of Preparing INDs and NDAs, The American Pharmaceutical Industry, etc.
  • Employment opportunities include:
    • Collecting data and preparing submissions to regulatory agencies
    • Assisting in the development of procedures to ensure regulatory compliance
    • Interfacing with regulatory agencies
    • Facilitating identification and resolution of scientific and regulatory issues with regulatory agencies, etc.
Fees componentsAmount
Tuition & fees2038489 INR
Hostel & Meals1011151 INR
Insurance245208 INR
Full-Time University Fee143111 INR
Total1399470 INR

Entry Criteria

Class 12thNo specific cutoff mentioned
BachelorsNo specific cutoff mentioned
  • Applicants must hold a bachelor’s degree from an accredited college or university are eligible to apply for admission
  • The program specializations in Pharmaceutics usually require an undergraduate degree in pharmacy, chemistry, biology, or a related science specialty
ExamsTOEFL: 79

IELTS: 6.5

GRE: Accepted
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