What should I know about existing CE marking and future requirements?
TORONTO (PRWEB)
October 05, 2021
Register for this webinar for a virtual panel discussion of some of the critical questions being asked about medical device requirements for global health authorities with special emphasis on EU EUDAMED. The panel will discuss topics like:
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What should I know about existing CE marking and future requirements? - For IVDR, who decides what class a product falls into and can I ‘self-certify’ under the IVDR?
- Are there some products that have resulted in reclassification to a ‘higher class’ for EU-MDR? What are some examples?
- When the UDI/Device Registration Module opens, will EUDAMED already be populated with existing ‘Directive’ device info? If I participate in the voluntary period, does that count as an ‘official’ submission or do I re-submit when EUDAMED goes live?
- For EUDAMED device registration, what is the difference between Regulation and Legacy requirements?
- What Quality Management changes need to occur to comply with MDR/IVDR?
- What are the main differences between GMDN and EMDN? Is mapping available between the two standards?
Join expert speakers from Reed Tech, Gary Saner, Sr. Manager, Information Solutions Life Sciences; and John Lorenc, Director Product Management, Medical Devices; as well as Mark Wasmuth, CEO, The GMDN Agency; Tom Rish, Medical Device Guru, Greenlight Guru; and Erin Salbilla, Director of Quality Systems, Vyaire Medical, in a live webinar on Thursday, October 21, 2021 at 11am EDT (4pm BST/UK).
For more information, or to register for this event, visit Preparing Data for EUDAMED: A Virtual Panel.
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