Device Week, Dec. 20, 2017 – Medtech Regulatory Landscape In 2018
Executive Summary
On this week's podcast, David Filmore discusses with Shawn M. Schmitt some of the important dynamics that will impact medtech regulations globally in 2018, with a focus on the US, Europe and Asia.
Listen to the podcast via the player below:
Medtech Insight content addressed in this episode:
- Interactive Timeline: Global Regulatory Deadlines
- 5 Ongoing US FDA Device Center Pilot Programs: A Listing
- A No-Predicate 510(k) Future? Pending US FDA Policy Might Forge A Path
- Expert Panel: How Manufacturers Are Paying For Notified Body Struggles
- Brexit Roundup: UK Medtech Balancing On A Fault Line
- India Settles On Classifications For Nearly 600 Devices, IVDs
- Malaysia Moves: Asian Medtech Associations Regulatory Networking November 2017, Part I