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Home > Programs > Master of Science In Regulatory Affairs for Drugs, Biologics, and Medical Devices
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Master of Science In Regulatory Affairs for Drugs, Biologics, and Medical Devices
Northeastern University has developed a unique graduate program that will address regulatory affairs within each category of regulated agents: drugs, biologics, and medical devices. Students will gain the regulatory affairs knowledge valued not only by RA departments, but also useful in medical product and pharmaceutical sales, marketing, and clinical investigations.
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As the field of Regulatory Affairs (RA) continues to grow, professionals with a thorough understanding of the complexities of medical product regulation and the role of the FDA are in greater demand. Northeastern University has developed a unique graduate program that will address regulatory affairs within each category of regulated agents: drugs, biologics, and medical devices. Graduates of the master's degree program will have the regulatory affairs knowledge valued not only by RA departments, but also useful in medical product and pharmaceutical sales, marketing, and clinical investigations.
The Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices is designed to educate and prepare RA professionals who will play a pivotal role in ensuring compliance with applicable laws and regulations in the development and commercialization of the healthcare products of their company.
While this program can be an excellent complement to those with health- or science-related degrees, there are many rewarding career opportunities with regulatory affairs for individuals with a variety of backgrounds. |
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