If you are in the medical device industry, are you prepared for the EU MDR?
In this on-demand webcast, Tech-Clarity’s Michelle Boucher interviews Caroline Byrd, regulatory expert at Abbott, about the steps Abbott has taken to prepare product data for EU MDR compliance. They discuss:
- Significant changes between the MDD and MDR
- How to prioritize the work required to ensure you have the product data to comply with the EU MDR
- Key roles and responsibilities to define to support the compliance efforts
- The role of technology, including PLM, to create a digital thread that will support complete submissions
The May 2020 deadline is approaching quickly. By viewing this webinar you will receive practical advice to help you on your journey to comply with the EU MDR.
