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:
- Demonstrate a mastery of a broad didactic foundation in regulatory affairs gained in advanced coursework;
- Develop strong skills through exposure to significant regulatory projects and case studies during which they translate their knowledge into practice; and
- Utilize professional skills such as statistical analysis, knowledge of regulatory guidance documents, as well as written and verbal communication skills.
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