FDA’s Medical Device Software Regulation Strategy

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November 19 - November 20

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.

Organizer

Complianceonline
Email:
referral@complianceonline.com

Venue

VIRTUAL SUMMIT