With all the new and proposed regulations in the past year, there is one thing you can bet on in 2017, change. From the new EU MDR and IVDR, to the new version of ISO 13485:2016, to the increased focus on risk management by regulatory bodies across the globe, you will need to begin preparing for it all. Specifically you will learn: - Expected changes coming at FDA (and how they affect you) - Quality inspection areas of concern - Steps you can be taking to prepare for the transition to ISO 13485:2016 - What to expect when it comes to the new EU MDR & IVDR - Tips on what to expect when putting together your FDA regulatory submission Watch the presentation here: https://www.greenlight.guru/webinar/2017-medical-device-industry-predictions