A checklist is the list of requirements to complete this program and receive the award, as the college publishes it in its catalog. It is the same for everyone. It does not say what you have completed; that comes from applying your own record.
Program
- Award
- Graduate Certificate
- Credential class
- ceterms:Certificate
- CIP
- 51.0720
- Catalog edition
- Catalog 2026-2027
- Checklist type
- degree-program
- Description
- 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.
Identifiers
- IPEDS UNITID
- 167358
- CourseShelf checklist
- CK_167358_b55a7deb
- CollegeTransfer.Net
- Institution Transfer Profile
- Source
- CourseShelf publish 61
Requirements to complete
Every course or condition the catalog lists, in the catalog's order.
Required Courses
4 items
- RGA 6600Introduction to Food and Drug Administration Pharmaceutical RegulationNot resolved to a course3
- RGA 6660Therapeutic Product Development: A Regulatory OverviewNot resolved to a course3
- RGA 6670Global Impact of Electronic Common Technical Document (eCTD) SubmissionsNot resolved to a course3
- RGA 6680Project Management in Early Drug Discovery and DevelopmentNot resolved to a course3
Source. Northeastern University, catalog Catalog 2026-2027 — https://catalog.northeastern.edu/graduate/professional-studies/graduate-certificate-programs/biopharmaceutical-regulatory-affairs-graduate-certificate-vtl/. Captured page pages/0329.html.gz. Assembled from the institution's published catalog as captured; every record names its captured page and source URL. Assembled, not asserted.