Eric Kupferberg, PhD
Senior Fellow and Faculty Member, MS in Regulatory Affairs for Drugs, Biologics and Medical Devices, Northeastern University
Do you want to learn more about the drugs, biologics, and medical devices regulatory environment? Join us for a Lunch & Learn on “Leading in the Field of Regulatory Affairs,” led by Eric Kupferberg, PhD, senior fellow and member of Northeastern’s MS in Regulatory Affairs for Drugs, Biologics, and Medical Devices program. Dr. Kupferberg teaches in the areas of healthcare markets and policy, FDA culture and behavior, and international biomedical topics. Come learn more about the role of regulatory affairs professionals in a medical product’s lifecycle—i.e. regulatory compliance and the preparation of submissions, project management, and market awareness. Also, hear how Northeastern students in the MS in Regulatory Affairs for Drugs, Biologics, and Medical Devices program are preparing for the field through opportunities such as co-op internships and career placement assistance.