Welcome to the Pacific Design & Manufacturing Presentation Store. Here you can view and download conference and/or show floor theater presentations before, during, and after the event. If you’re looking for a presentation from a specific session that you’re unable to find here, note that it’s likely because the presenter has not provided permission for external use or has not yet shared their presentation with us. Please check back after the event for a more complete catalogue of available presentations.
Isabelle Lang-Zwosta (Global Regulatory Affairs and Business Development Dr. med. (MD) , knoell Germany GmbH)
Location: Booth 637
Date: Thursday, February 13
Time: 10:30 am - 11:15 am
Track: Tech Theater
Vault Recording: TBD
Audience Level: All
The new EU Medical Device Regulation (MDR) is set to go into effect May 26, 2020. With less than half a year until the MDR takes effect, it is time to address the CE transition to MDR right away. Our experts developed a last minute checklist than enables you to take action to prevent a disruption of distribution of your medical devices in the EU. During this session we will discuss the most crucial endpoints, the toughest deadlines and help you getting a clear picture on what's to be done by May 2020.