Master of Science in Regulatory Science (MSRS)
The MSRS degree requires 12 credit units including coursework and a thesis.
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 Trial Management
- REG 6120 — Introduction to Drug Development
- REG 6180 — Introduction to Vaccine Development
- 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 6240 — Applied Regulatory Processes of Vaccines and Biologics
- PHRM 6230 — Fundamentals of Pharmacology
- PHRM 5900 — Toxicology
- 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 |
|
REG 6020 Proposal Development REG 6040 Scientific and Ethical Conduct |
REG 6000 Biostats REG Core 1 |
REG Core 2 Elective 1 |
|
| Year 2 |
Summer |
Fall |
Spring |
|
REG 6100 Fundamentals of FDA Regulation |
Elective 3 |
REG 9910 Thesis I REG 9911 Thesis II |
|
|
ASCEND Professional Development Series |
|
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.