November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, MinnesotaNovember 5 - 7, 2024
The Royal Sonesta Minneapolis Downtown,
Minneapolis, Minnesota
The Royal Sonesta Minneapolis Downtown,
Minneapolis, Minnesota
EU MDR Implementation
Notified Body Feedback. Industry Case Studies. Post Market Surveillance. Clinical Requirements
highlights include:
The very latest on EU MDR Implementation
- Best practice EU MDR implementation industry case studies from Alcon and BTG International
- Assess the common implementation challenges faced by manufacturers in our interactive panel discussion
- Hear Notified Body and Competent Authority feedback on implementation so far
Gain answers to the questions keeping you awake at night
- Will your Notified Body have sufficient capacity and resource? When and how can you switch your Notified Body?
- ISO13485:2016 – Quality Management Systems QMS) and the MDR: what’s new and how can you prepare?
- What are the expectations for clinical evaluations and investigations under the MDR?
Best practice industry perspectives and Notified Body insight from:
- Medtronic
- BD
- Alcon
- GMED North America
- Zimmer Biomet
- Abbott
Get the Latest Event Updates
Sign up to get the latest event updates and information.