Overview
The Regulatory Affairs programme at the University of Georgia provides a comprehensive education in the legal and scientific frameworks governing the pharmaceutical and biomedical industries. This non-thesis M.Sc. is specifically designed for professionals seeking to manage compliance and product approval processes in a rapidly evolving global market. Students gain the technical expertise required to navigate complex policies across various healthcare sectors.
Why Regulatory Affairs at University of Georgia?
The University of Georgia College of Pharmacy is ranked 15th in the nation by U.S. News & World Report, reflecting its status as a premier institution for pharmaceutical education. The programme is delivered through the Institute for International Biomedical Regulatory Sciences, offering a curriculum that addresses the expansion of the biotech and medical device industries. Students benefit from a flexible online structure that allows them to maintain professional commitments while gaining specialised knowledge from a top-tier research university.
Tuition Fee Breakdown
- International fee: USD 30182 per year
- National fee: USD 30182 per year
- Local fee: USD 9808 per year
Visit the Fees and Funding section for a breakdown in your local currency.
Syllabus
The curriculum consists of at least 39 credit hours, focusing on the lifecycle of medical products and international legal requirements. Modules may include:
- Pharmaceutical, Biotechnology, and Device Industries
- Food and Drug Law
- Current Good Manufacturing Practices
- Ethical Issues in Research
- U.S. Marketing Applications
- Biostatistical Applications
- Quality Control and Quality Assurance
- Medical Device Development
- Clinical Trials Design and Management
Careers with Regulatory Affairs
Graduates are prepared for leadership roles within industry, government, and academia, often serving as vital liaisons between companies and regulatory authorities. The programme equips students for careers in the regulation, manufacturing, and marketing of pharmaceuticals, biologics, and in-vitro diagnostics. Common career paths include regulatory management and compliance oversight for international medical device and veterinary product corporations.
Programme Structure
- To obtain additional information about the program, we kindly suggest that you visit the programme website, where you can find further details and relevant resources.
Key information
Duration
- Part-time
- 12 months
Start dates & application deadlines
- Starting
- Apply before , International
- Apply before , National
-
- Starting
- Apply before , International
- Apply before , National
-
Language
Credits
Delivered
Campus Location
- Lawrenceville, United States
Disciplines
Pharmacy Health Sciences View 473 other Masters in Health Sciences in United StatesWhat students do after studying
Academic requirements
We are not aware of any specific GRE, GMAT or GPA grading score requirements for this programme.
English requirements
Other requirements
General requirements
- Admission and Application Procedures
- Readmission Procedures
- Deferring an Application
- Application Fee
- Transcripts and Academic Records
- Entrance Test Scores
- Letters of Recommendation
- Non-Degree or Transient Status
- Application Forms
- Summary of Materials
Tuition Fees
-
International Applies to you
Applies to youNon-residents30182 USD / year≈ 30182 USD / year - Out-of-State30182 USD / year≈ 30182 USD / year
-
Domestic
Applies to youIn-State9808 USD / year≈ 9808 USD / year
Funding
In order for us to give you accurate scholarship information, we ask that you please confirm a few details and create an account with us.
Scholarships Information
Below you will find Master's scholarship opportunities for Regulatory Affairs.
Available Scholarships
You are eligible to apply for these scholarships but a selection process will still be applied by the provider.
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