GAO Calls for Stronger FDA Oversight of Third-Party Medical Device Reviews
A federal watchdog report highlights audit delays exceeding six months for accredited organizations handling 510(k) reviews for low-to-moderate risk devices.
HTM’s Headlines
Editor's Picks
Cyber Resilience Program Puts Clinical Continuity in HTM’s Sights
Joint Commission and AHA leaders say hospitals should be prepared to sustain patient care for weeks when critical technology and connected medical equipment are unavailable.
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Join our mailing list to receive the latest news, information, and updates in the BioMed and HTM market.Critical Resources
Protecting Patient Data
Continuous Compliance for Connected Medical Devices: Reducing the Time From Change to Response
How to update cybersecurity assessments and controls between scheduled reviews.
Staffing Essentials
Facility Fundamentals
Device Management 101
A Digital Twin for the Linac: Testing Fixes Before Touching the Machine
Linax Technologies' new SIMAC platform lets service engineers model beam behavior, trace anomalies, and train on a virtual linac without competing for vault time.