MS in Regulatory Affairs
The MS in Regulatory Affairs programme provides students with the essential knowledge and skills required to help companies navigate an increasingly complex regulatory environment. It enables students to acquire the foundation necessary to work within a variety of fields, including medical product development, pharmaceutical sales, strategic marketing, and clinical investigations. The course focuses on examining every step of the drug development and regulation process and analysing how emerging developments reshape medical regulations.
Cost of Living: USD 16,000 per year
- Summer Semester - 8 May
- Fall Semester - 18 July
- Online Application
- Unofficial Undergraduate Transcripts
- Statement of Purpose
- Two Letters of Recommendation
- Resume or Curriculum Vitae
- English Language Proficiency
- TOEFL - 79
- IELTS - 6.5
- PTE - 53
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