MS in Regulatory Affairs

Earn your Master of Science in Regulatory Affairs (MSRA) and learn directly from industry professionals in Irvine, CA. You will gain the skills to navigate the complex regulatory landscape of pharmaceuticals and medical devices, driving the development and approval of innovative healthcare products.

Technician in pharmacy lab.

Why an MS Regulatory Affairs at Chapman University?

The Master of Science in Regulatory Affairs (MSRA) is a four-semester hybrid program that combines online learning with hands-on simulation and training. You will build advanced skills to become a knowledgeable and effective leader in regulatory affairs.

Career Opportunities

Learn from faculty with decades of real-world experience in industry and regulatory affairs. At Chapman’s Rinker Campus in Irvine, you will study in the heart of a thriving biomedical hub, gaining access to a dynamic healthcare network and exploring diverse career paths to understand how medical products reach the market in the U.S. and worldwide.

Specialized Training

As a graduate of the Master of Science in Regulatory Affairs program, you will be ready to step into impactful roles in the biopharmaceutical, medical device, and diagnostics industries. You will gain specialized training in global regulatory strategy, clinical trial oversight, and FDA compliance to launch and grow your career.

Expert Faculty Mentorship

You will explore topics such as medication therapy management, prescription drug misuse, pharmaceutical intellectual property, and FDA policies and regulations.

Industry Connections

You will benefit from guidance by our Professional Advisory Board, whose members hold senior leadership roles at Johnson & Johnson, Applied Medical, aTyr Pharma, Edwards Lifesciences, Masimo, and AbbVie.

Attallah Ph.D. in Education
Duration
Full-time
Application deadline(s)

Priority Consideration:

January 15, 2026

 

Regular Deadline:

June 30, 2026

 

*Applications received after the deadline will be considered on a space-available basis

Tuition
Format
Hybrid
Scholarships available

Scholarships are available through general Chapman graduate financial aid.

Start semesters
  • Fall: mid-late August
  • Spring: late January-early February

Chapman University School of Pharmacy

Impact the health of your community with a degree from Chapman University School of Pharmacy, where excellence is the standard. Our innovative approach to preparing leaders in health care through research, interdisciplinary and experiential learning, and hands-on guidance from caring faculty will provide you with the education and skills needed to launch your pharmacy career.

Hear from our Students/Alumni

Faculty Spotlights

Our distinguished faculty bring research expertise and a commitment to mentorship, guiding students to connect theory with real-world impact.

Dr. Marc Fleming

Dr. Marc Fleming

Professor; Chair, Department of Pharmaceutical Economics and Policy
Expertise: Pharmaceutical economics and policy with research focus on medication therapy management, prescription drug misuse prevention, and pharmacist behavior in pain management and opioid misuse prevention.
Dr. Enrique Seoane-Vazquez

Dr. Enrique Seoane-Vazquez

Professor

Research Interests: Pharmaceutical economics, regulation and policy, FDA regulatory actions, generic drug markets, drug utilization and safety, and health economics with a focus on cost-effectiveness of medications and healthcare interventions.

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Career Outcomes

Frequently Asked Questions

What is the MS in Regulatory Affairs program?

A four-semester hybrid program combining online learning and on-campus sessions focused on global regulatory strategy, clinical trials, and FDA compliance.

Who is eligible to apply?

Professionals or graduates who hold at least a bachelors in science, pharmacy, engineering, law, or related fields seeking careers in regulatory affairs for medical products.

Where is the program offered?

At Chapman’s Rinker Health Science Campus in Irvine, located within Southern California’s biomedical hub.

What careers can graduates pursue?

Roles in the biopharmaceutical, medical device, and diagnostics industries, including regulatory specialist, compliance manager, or clinical affairs associate.

When are applications due?

Applications open each July with a January 15 priority deadline and June 30 final deadline for the fall intake. Applications submitted after the deadline will be reviewed on a case-by-case basis.