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
EU Pharma Package: Sharp New Tools With Limited ProtectionsDecember 19, 2025EU Pharma Package: Sharp New Tools With Limited ProtectionsDecember 18, 2025EU Biotech Act: EU Proposes First Set of Rules to Facilitate Biopharmaceutical CompetitivenessThursday, December 18, 2025U.S. Drug Pricing Year in Review: Reflections on 2025 and Getting Ready for 2026December 12, 2025Sidley Represents Immunovant in US$550 Million OfferingDecember 12, 2025BIOSECURE Act Included in the FY2026 National Defense Authorization ActDecember 12, 2025
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory
