This is Canada’s only master’s degree in regulatory affairs, focused on the development and commercializationof drugs, biologics, and medical device products.
Key differentiators of our program:
Six unique concentrations: Operational Regulatory Affairs, Strategic Regulatory Affairs, Clinical Research Regulatory Affairs, International Regulatory Affairs, Regulatory Compliance, or General Regulatory Affairs.
Choose the learning format that meets your needs (100% online or flexible hybrid format that combines online and in-class instruction).
Experiential learning: Acquire hands-on experience through in-the-field research, capstone projects, co-op opportunities, or integrative learning experience at your current employer.
Admissions at the College of Professional Studies operates on a rolling basis, meaning that applications are reviewed as they are received, and there are multiple intakes over the course of the academic year. See below for upcoming academic terms along with the application deadline for each.
Why Regulatory Affairs?
The Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices program is designed to produce graduates who are highly qualified to manage the regulatory process for companies innovating and developing cutting-edge products in science and medicine.
Ever-changing laws and regulations are driving demand for regulatory affairs professionals who can help companies effectively bring medical products to market. To prepare you to effectively manage regulatory activities, Northeastern University’s College of Professional Studies offers the online Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices. This unique graduate degree is designed to deepen your understanding of current regulations and their practical application in the development and commercialization of drugs, biologics, and medical device products.
Regulatory affairs courses within this program will provide you with the integrated knowledge and broad perspectives you need to effectively manage the regulatory process. From discovery to commercialization, this regulatory affairs master’s degree will cover the steps that are required to bring a medical product to market, both in the U.S. and around the globe. Delivered entirely online, graduate courses address critical regulatory issues affecting all of the stages and processes in regulatory affairs.
Northeastern’s MS in Regulatory Affairs for Drugs, Biologics, and Medical Devices offers students the opportunity to meet their career goals in the fields of regulatory affairs — such as operational and strategic regulatory affairs, clinical regulatory affairs, and regulatory compliance — by focusing their education in one of eight unique concentrations that span the entire discipline. Concentration offerings include:
Clinical Research Regulatory Affairs
General Regulatory Affairs
International Regulatory Affairs
Operational Regulatory Affairs
Strategic Regulatory Affairs
Medical Device Regulatory Affairs
Quality Assurance and Compliance
Non-clinical Biomedical Product Regulation
Gain the essential knowledge and skills required to help companies navigate an increasingly complex regulatory environment.
Acquire the foundation necessary to work within a variety of fields, including medical product development, pharmaceutical sales, strategic marketing, and clinical investigations.
Examine every step of the drug development and regulatory process.
Sharpen your understanding of the laws that govern the development, manufacturing, and commercial distribution of drugs, biologics, and medical devices.
Analyze how emerging developments and trends are reshaping medical device regulations.