November 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
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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
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