Graduate Certificate in Biopharmaceutical Regulatory Affairs at Northeastern University

The biotechnology and pharmaceutical industries continue to experience rapid growth in the U.S. market. As companies in these industries seek approval to market their products in the United States, demand for qualified regulatory affairs professionals continues to increase. Product development scientists, marketers, quality personnel, and legal experts who guide companies through the Food and Drug Administration approval process will benefit from regulatory affairs training. Offered at: Boston, Online.

Faculty: College of Professional Studies  |  Department: Graduate Certificate Programs  |  Duration: 12 semester hours  |  Study mode: full-time  |  Location: Boston, MA, United States

What you will study

Requires 12 semester hours. Required courses include RGA 6600 Introduction to Food and Drug Administration Pharmaceutical Regulation; RGA 6660 Therapeutic Product Development: A Regulatory Overview; RGA 6670 Global Impact of Electronic Common Technical Document (eCTD) Submissions; RGA 6680 Project Management in Early Drug Discovery and Development.

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