The growth of the medical software industry outpaces the design of FDA's regulatory process. In some instances clinicians have weighed the risk of software failure against the benefits of using a device at all. Device software is often used in conjunction with other software-based devices, but their interoperability was never anticipated.
This seminar will focus on addressing these concerns and educating participants on FDA’s recent medical device software regulation strategies.
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Who Will Benefit:
Note: Use coupon code < GET20 > and get 20% off on registration and this offer is not valid for with stay registration.