On this week's podcast, David Filmore discusses with Shawn M. Schmitt some of important dynamics that will impact medtech regulations globally in 2018, with a focus on the US, Europe and Asia. For more information about Medtech Insight and to sign up for a free trial go to bit.ly/2w7LnlR.

Medtech Insight content addressed in this episode:

Interactive Timeline: Global Regulatory Deadlines: http://bit.ly/2An8xn8

5 Ongoing US FDA Device Center Pilot Programs: A Listing: http://bit.ly/2kmlx71

A No-Predicate 510(k) Future? Pending US FDA Policy Might Forge A Path: http://bit.ly/2BAuVLT

Expert Panel: How Manufacturers Are Paying For Notified Body Struggles: http://bit.ly/2iuUMfp

Brexit Roundup: UK Medtech Balancing On A Fault Line: http://bit.ly/2D9qvvS

India Settles On Classifications For Nearly 600 Devices, IVDs: http://bit.ly/2B1hVhe

Malaysia Moves: Asian Medtech Associations Regulatory Networking November 2017, Part I: http://bit.ly/2AY4nCX