Skip to main content
Med-Tech Innovation News

How Software May Be Classified Under Medical Device Regulation Guidance

November 11, 2019
Authors
Maria Isabel ManleyZina Chatzidimitriadou

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

View Article

Contacts

Manley, Maria Isabel
合伙人律师
Chatzidimitriadou, Zina
资深主办律师

Capabilities

Suggested News & Insights

Bay Area Life Sciences RoundtableWednesday, July 22, 2026
活动
Sidley & Life Science Cares Reception at BIO 2026Monday, June 22, 2026
活动
Boston Life Sciences RoundtableTuesday, June 9, 2026
活动
Sidley Sponsors the 2026 EU Pharma Law ForumTuesday, May 19, 2026 – Thursday, May 21, 2026
活动
Women’s Life Sciences Network – Biotech Act: Funding and Investment OpportunitiesTuesday, May 19, 2026
活动
Growth Meets Guardrails: Getting You Ready for the New Realm of Ad/PromoWednesday, May 13, 2026
活动