MD&M East

EU Devices Directive Changes Not Radical, but Not Insignificant

Linda Horton says changes won't affect U.S. companies much. Although changes to the European Union's Medical Devices Directives probably won't involve a major overhaul of the regulations or the system ...
Yahoo Finance

EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) Training Webinar: Explore Impact on Regulatory Strategies, and Practical Steps for Achieving Compliance

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "EU MDR and IVDR: Key Updates and Compliance Strategies for 2025 (Aug 6, 2025)" training has been added to ResearchAndMarkets.com's offering. The EU ...
BioWorld

Stereotaxis receives CE mark certification for devices in Europe

Stereotaxis Inc. recently received CE mark recertification for all its devices currently available in Europe under the new Medical Device Regulation (MDR) regulatory framework. The MDR has replaced ...
Business Wire

Neo Medical’s Spine Care Platform Fully Approved Under EU Medical Device Regulation Directive

LAUSANNE, Switzerland--(BUSINESS WIRE)--Neo Medical SA (Neo), a Swiss technology company specializing in spine surgery, today announced the approval of its entire product portfolio under the European ...
HealthTech

MDR Medical Device Regulations: A Safety Net or Too Much Restriction?

The European Union’s Medical Device Regulation (MDR) is a complex regulatory framework created to put in place rules and requirements in how medical devices are designed, manufactured, and marketed.