In this Hangout, we will discuss the basic concepts of medical device regulation in the U.S., what is considered significant risk versus non-significant risk, and how the level of risk factors into the regulation of new product development.﻿

https://plus.google.com/u/0/events/cqba9srrpgjbbseq0dechrhfsk4

Jenny Romaine

DC/MD/VA Biotechnology Group

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NHLBI: Conquering the (Regulatory) Basics - Medical Device Classification

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DC/MD/VA Biotechnology Group

NHLBI: Conquering the (Regulatory) Basics - Medical Device Classification

DC/MD/VA Biotechnology Group

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