[Webinar]Preparing for the New EU Medical Device Regulation
The upcoming European Union (EU) Medical Device Regulation (MDR) will replace the Medical Devices Directive and the Active Implantable Medical Devices Directive. Travis Miller, Assent’s General Counsel, will discuss the new requirements under the regulation and what companies need to do to prepare their programs.
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[Webinar] Preparing for the New EU Medical Device Regulation 181205
11AM ET | 8AM PT | 3PM GMT
Wednesday, December 5th, 2018
Approximately 60 minutes
Topics to be covered in this webinar include:
- The differences between the EU MDR and the directives it will replace
- Reporting requirements under the EU MDR
- How to update technical documentation to comply
- Which processes to implement to meet the new requirements
Don’t miss this opportunity to learn about the new requirements and how to prepare your program!