BNG 528: Med Dev Regs & Regltry Strats

Discussion of the laws and regulations applied to medical products development, manufacturing, testing, marketing, and post-marketing surveillance. This course provides an overview of regulatory affairs related to biomedical devices and a foundation to understand the differences in regulations between countries with a focus on the US FDA requirements. This course also teaches risk management about medical products.

Course information

3.00 credits
Section 01: Graduate Lecture
Instructor(s): 

Class: #11659

Tue, Jan 21, 2020 - Wed, Apr 29, 2020

Status: 

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