Explore FDA's QMSR and cybersecurity mandates for medical devices, including SPDF, SBOMs, and legacy medical device ...

The medical device industry stands at a critical inflection point. As healthcare costs continue to spiral upward and demands for transparency intensify, the need for comprehensive asset visibility and ...

DUBLIN--(BUSINESS WIRE)--The "Risk Management in Medical Devices Industry" conference has been added to ResearchAndMarkets.com's offering. Risk management is a mandatory and necessary process during ...

February 10, 2026 - PRESSADVANTAGE - Language Scientific has shared an overview of common risks in translations for ...

DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products" conference to their offering.

The company advances precision CNC machining for medical device components with ISO 13485–aligned quality control and ...

INDIANAPOLIS, Nov. 25, 2019 /PRNewswire-PRWeb/ -- Greenlight Guru, the only medical device quality management system (MD QMS) software platform, today announced findings from the "State of Medical ...

Draft guidelines aim to align India's medtech software framework with global practices; industry seeks more clarity on AI/ML evaluation and algorithm change management: CDSCO guidelines ...

Revolutionizing Operating Room Efficiency and Patient Care with Cutting-Edge Electric Hydraulic Technology CALIFORNIA, ...