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.

Duration Duration: 1-2 years | Type: Masters
Tuition Fee: USD 37,800 per year
Cost of Living: USD 16,000 per year
Admissions Admissions
  • Summer Semester - 8 May

  • Fall Semester - 18 July

Documents Required Documents Required
  • Online Application

  • Unofficial Undergraduate Transcripts

  • Statement of Purpose

  • Two Letters of Recommendation

  • Resume or Curriculum Vitae

  • English Language Proficiency

Test Type & Score Test Type & Score
  • TOEFL - 79

  • IELTS - 6.5

  • PTE - 53

MS in Regulatory Affairs

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