Med-Tech Innovation News
How Software May Be Classified Under Medical Device Regulation Guidance
November 11, 2019
Authors Marie Manley and Zina Chatzidimitriadou discuss how software will be classified under the new European medical device framework.
Originally published in Med-Tech Innovation News – November 11, 2019
Contacts
Capabilities
Suggested News & Insights
Life Sciences College 2027Thursday, February 4, 2027Exclusive Fireside Chat: A Conversation With FDA's Chief CounselTuesday, January 12, 2027Recharge & Recaffeinate With Sidley @ JPMMonday, January 11, 2027 – Tuesday, January 12, 2027GMP 2026: Regulatory Reliance, AI, and the Future of Pharmaceutical ManufacturingWednesday, December 2, 2026Sidley Senior Managing Associate Jason Hyatt to Speak at PwC Life Sciences IPO Readiness WorkshopMonday, November 16, 2026What Does It Take to Build a Business Around a Single Patient? Emerging “N-of-1” Models and the Regulatory Road AheadNovember 13, 2026
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory