Program Overview
The Master of Engineering in Regulatory Biomedical Engineering (RBME) is an interdisciplinary program offered through the Department of Biomedical Engineering in partnership with GW's School of Medicine and Health Sciences. The new program addresses an unmet need for a graduate program to train engineers in the specific set of skills of regulatory science, biomedical innovation, and entrepreneurship.
Students with training in engineering or physics and/or relevant industry/government experience study the fundamentals of biomedical engineering, global regulatory affairs, regulatory strategy in the development of devices and diagnostics, regulatory compliance, engineering patent law, medical measurements, and instrument design.
In addition to coursework, students gain experience in SBIR/STTR grant applications and/or FDA Premarket Notification (510(k)) submissions for medical devices.
Program Outcome
Students who complete the Master of Engineering in Regulatory Biomedical Engineering acquire skill sets comparable to those of an engineer with five to seven years of experience, making them competitive in the medical device or imaging industries. Graduates will be equipped to provide in-house regulatory expertise to device companies, or join government regulatory and compliance institutions.
Curriculum
The RBME program is 30 credit hours distributed across four areas:
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Esperado Janeiro 2025
George Washington University
1918 F Street, NW,
WASHINGTON,
District Of Columbia,
20052, United States
To be eligible for admission, applicants must hold a Bachelor's degree from a regionally accredited college or university. Applicants who have earned their degrees outside of the US must hold degrees from institutions in compliance with their national standards.
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