Master of Science in Regulatory Science (MSRS)
The MSRS degree requires 12 credit units including coursework and a thesis.
- MSRS Curriculum Structure
- Course Plan (10 c.u.)
- Thesis (2 c.u.)
Structure of Curriculum
Required Core (4)
- REG 6000 — Intro Biostats
- REG 6020 — Proposal Development and Study Design
- REG 6040 — Scientific & Ethical Conduct
- REG 6100 — Fundamentals of FDA Regulation
Regulatory Core (2)
- REG 6110 — Clinical Study Management
- REG 6120 — Intro Drug Development
- REG 6300 — Clinical Trials
- REG 6140 — Biopharmaceutical Development, Manufacturing and Regulatory Affairs
- REG 6150 — Post-Approval Maintenance of Drugs, Devices, and Biologics
Thesis (2)
- REG 9910 — Thesis I
- REG 9911 — Thesis II
Electives (4)
For Example:
- REG 6201 — Cell and Gene Therapy
- REG 6230 — Fundamentals of Pharmacology
- REG 5900 — Toxicology
- MTR 6010 — Review Writing
- MTR 6030 — Disease Measurement
- MTR 6050 — Data Manuscript Writing
- MTR 6060 — Grantmanship
- MTR 9990 — Lab (up to 2 c.u., including internship option)
Study Plan
| Year 1 |
Summer |
Fall |
Spring |
PSDP |
|
REG 602 Proposal Development REG Core 1 |
REG 600 Biostats REG Core 2 |
REG 604 Scientific and Ethical Conduct Elective 1 |
||
| Year 2 |
Summer |
Fall |
Spring |
|
|
REG 610 Fundamentals of FDA Regulation |
Elective 3 |
REG 9910 Thesis I REG 9911 Thesis II |
Disclaimer
Please note that policies concerning admissions, curriculum, funding and financial aid are subject to change. Additionally, though variations in the curriculum may be possible, any changes will need prior approval and may have financial implications. This website is meant to provide preliminary general overview information only. Students interested in or enrolled in the program should seek personal advising from relevant faculty and staff.