FDAs Medical Device Software Regulation Strategy: 2-Day In-Person Seminar by Ex-FDA Official

The growth of the medical software industry outspaces 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.

Th ...

Last Published: December 22, 2014 by Jim

Category: Healthcare and Medical