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Advance your knowledge of the required laws, policies, and regulations covering drugs, medical devices, and biologics.

This program, which combines online and in-person learning opportunities, takes approximately two years to complete. In that time, you will learn from experts in drugs, devices, biologics, healthcare, and policy. You will gain the knowledge and experience to navigate and uphold the regulatory and legal environment in vital capacities, such as helping pharmaceutical companies gain FDA approval or assisting regulatory agencies in developing healthcare policies. When you graduate, you will be fully prepared to advance as a leader in the industry. You may begin this flexible program in the fall, spring, or summer semesters.

Your Educational Journey

The MCPHS Master of Science in Regulatory Affairs and Health Policy consists of required and elective courses that provide essential knowledge in all areas of this field. Courses include:

Law and Health Policy of Drugs and Devices
FDA and Regulatory Affairs
Health Epidemiology
Pharmaceutical Economics and Policy
Statistics in Clinical Research
Laws and Regulations Governing Human Research
Principles of Quality Assurance and Control