Major in Drug Regulatory Affairs
The University of Florida offers a 30-credit part-time online concentration in Drug Regulatory Affairs as a track within the Pharmacy Regulation and Policy masters program, using some coursework from the Applied Pharmacoeconomics, Patient Safety and Risk Management, and Clinical Research and Risk Management programs. This track is a flexible opportunity to customize the educational experience of those who are already in the drug regulatory affairs area, or those who wish to transition into drug regulatory affairs from another specialty.
Courses in the curriculum:
- Structure, Process & Outcomes of Regulation
- Federal Regulation of Drugs & Pharmacy
- Federal Regulation of Controlled Substances
- Research Methods
- Regulating Pharmaceutical Access and Cost
- Ethics in Drug Production, Distribution and Use
- Patient Safety Program Evaluation
- Evidence-Based Medicine
- Pharmaceutical Health Economics
- Pharmacoepidemiology
- Pharmaceutical Products and Public Policy
- Use and Abuse of Statistics
- Regulation of Clinical Research
- Health Care Risk Management
- Practices & Procedures of Administrative Agencies
- Patient Responsibility in Health Care
- Health Care & Patient Safety
- Pharmaceutical Outcomes & Policy Seminar
Schedule
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Spring Semester (January) Starters |
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August – October |
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January – February |
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November – |
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March – April |
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March – April |
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August – October | ||||
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November – |
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August – October |
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January – February | ||||
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November – December |
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March – April | ||||
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January – February |
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August – October | ||||
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March – April |
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November – December |
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Students also take three one-credit weekend seminars in residence at the UF main campus in Gainesville. Seminars are offered once each fall and spring. During the four years of the program, students have the opportunity to attend four seminars and must attend three of the four. On a case-by-case basis, students may apply to take a one-credit independent research project as a substitute for one of the seminars.
