Regulatory Practices in Biomedical Engineering

This course is an introduction to domestic and foreign regulatory practices associated with biomedical devices and/or products. It will cover the basics of the processes and protocols used by the FDA in order to better prepare students to be significant contributors to the development of a biomedical product that meets or exceeds all the applicable standards, regulations, and laws that apply to its applicable technology.

Term 202440 #42825 BME11453
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Instructor
Meeting Times
Location: JAMES 3091A (M)
@ 15:30 - 16:45
From 2024-09-03 to 2024-12-19
Enrollment

5

seats available

25

currently enrolled

30

maximum enrollment

Section Tally

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