MS&E Technology Assessment and Regulation of Medical Devices
Intellectual Property: Patent Law
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Technology Assessment and Regulation of Medical Devices
School of Engineering
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[ Academia ] [ Litigation ] [ Regulatory & Policy ] [ Transactional ] Intellectual Property: Patent Law
Why it is relevant for ...
[ Academia ] [ Litigation ] [ Regulatory & Policy ] [ Transactional ] as a Relevant Course outside SLS for those interested in Lifesciences: Innovations : Students interested in lifesciences should consider taking 1 or more courses on the market and regulatory issues raised by innovation in the IP and health care industries. This course addresses key components of product commercialization for medical technologies: regulatory approval and reimbursement by relevant payers in the system.
General course Description:
(Formerly 475.) Regulatory approval and reimbursement for new medical technologies as a key component of product commercialization. The regulatory and payer environment in the U.S. and abroad, and common methods of health technology assessment. Framework to identify factors relevant to adoption of new medical devices, and the management of those factors in the design and development phases. Case studies; guest speakers from government (FDA) and industry.
Course Style: A Substantive course teaches the law, theory, and policy in a particular area of law