The decision to amend the Regulation relieves pressure on national authorities, Notified Bodies, manufacturers, and other stakeholders. Don’t be fooled, this is no time to relax your efforts to prepare.

Do you have a submission strategy, even with the updated proposed timeline?

• What is the common feedback on EU MDR submissions?
• What are common requests from auditors during reviews?
• What is the European database on medical devices and why is it important?

Come to quiz Renee, Jai & Mark on this ever-changing topic.

Date: Thursday, April 20^th, 2023
Time: 6:00 pm CST – 8:00 pm CST
Location: St. Cloud State – Plymouth 9750 Rockford Road, Plymouth MN
Cost: Minnesota ASQ Member – $20.00
Non-Members – $40.00REGISRATION LINK: events.eply.com/EUMedicalDeviceRegulationYourQuestionsAnswered3370927

• A light snack will be provided.
• Certificates of Completion: Issued via email, after workshop completion, for .2 ASQ RUs or CEUs.</