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EU MDR Virtual Workshop Registration
June 10, 2020 @ 9:00 am - 1:00 pm
One event on June 17, 2020 at 9:00 am
One event on June 18, 2020 at 9:00 am
Join leading global experts as they guide you through the key elements of an actionable plan for keeping your medical devices on the EU market using proven strategies and successful practices. At this workshop, learn and develop plans to:
- Manage concurrent MDD and MDR compliant products, as well as assess the effects of any changes.
- Ensure market continuity for “Legacy” products after May 2021.
- Implement and coordinate post-market data and analysis for proper reporting and trending for mandatory submissions, as well as for compliant QMSs.
- Heighten awareness of the urgency to take action and gain support from senior leaders (CEO, COO, CQO, CFO, Chief Legal Officer, etc.).
- Effectively manage MDR Annex I – General Safety and Performance Requirements (GSPRs).