Why Post-Market Surveillance Is the Real Test of Medical Device Safety
Effective post-market surveillance depends on HTM teams to bridge the gap between regulatory oversight and real-world performance.
Effective post-market surveillance depends on HTM teams to bridge the gap between regulatory oversight and real-world performance.
ECRI is applauding the Centers for Medicare and Medicaid Services’ new Patient Safety Structural Measure, urging healthcare institutions to adopt a systems-based approach to improve safety and reduce preventable harm.
ECRI named AdventHealth Zephyrhills and AdventHealth Dade City hospitals in Pasco County, Fla., winners of the 2023 Safety Excellence Award.
Mountain View, Calif.-based Zingbox has released the findings of its second annual Healthcare Security Survey. The survey revealed a contradiction between the confidence that healthcare professionals have in the visibility of connected medical devices and security of their networks, and the inefficient legacy processes many still rely on to keep them secure.
The Medical Imaging & Technology Alliance (MITA) has announced the publication of NEMA/MITA 2—Requirements for Servicing of Medical Imaging Equipment, a voluntary standard outlining MITA’s minimum quality management system requirements for medical imaging device servicing.
The remote and predictive maintenance of medical devices is becoming more prominent due to the growing digitalization and device connectivity, market researchers say.
Getinge is recalling IABP devices due to a compromised intra-aortic balloon causing blood to enter the IABP during therapy.