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: a) Demonstrate a mastery of a broad didactic foundation in regulatory affairs gained in advanced coursework; b) Develop strong skills through exposure to significant regulatory projects and case studies during which they translate their knowledge into practice; and c) Utilize professional skills such as statistical analysis, knowledge of regulatory guidance documents, as well as written and verbal communication skills. These abilities will be acquired through specific coursework and seminars and other professional and personal development offered during the course of study.

Undergrad transcripts Statement of purpose 2 letters of recommendation Resume TOEFL/IELTS score