In this webinar, you will learn how to classify medical devices according to EU MDR 2017/745 Annex VIII for full compliance with new EU Medical Device Regulation mandatory starting 26-May-2021
Why Should You Attend:
New EU Medical Device Regulation (EU MDR) 2017/745 will be mandatory starting 26-May-2021. One of the first key steps to ensure CE mark for the device (that will allow EU market commercial activity) is the appropriate classification of the medical device following Annex VIII rules of the new MDR.Areas Covered in the Webinar:
- Rules
- New elements
- Decision trees
- Reclassified devices
- Devices without medical purpose
- Spine implants
- Take away
- Case studies
Who Will Benefit:
- Medical device industry Regulatory Affairs
- Regulatory Compliance and Quality Assurance Managers
- Directors and VPs.
Course Provider
Juan M Campos,
