Medical Innovation Exchange

collaboration

How to Thrive Amid the Shifting Sands of Medical Device Regulations

How to Thrive Amid the Shifting Sands of Medical Device Regulations     Emerging issues around artificial intelligence (AI), telehealth and data privacy have triggered a surge in regulatory action. This trend is both a challenge and an opportunity. Companies that can adapt quickly to meet regulatory shifts could surge ahead of the competition. Here’s how …

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The Underrated Variable of IoMT Device Security: Collaboration

The Underrated Variable of IoMT Device Security: Collaboration     Healthcare delivery organizations face significant operational risks (at best) and dangerous patient outcomes (at worst) if they fail to sufficiently secure internet-connected devices and equipment across their entire lifecycles. To put some rather eye-opening numbers to it: a recent Ponemon Institute survey revealed that more than …

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The Underrated Variable of IoMT Device Security: Collaboration

The Underrated Variable of IoMT Device Security: Collaboration     Healthcare delivery organizations face significant operational risks (at best) and dangerous patient outcomes (at worst) if they fail to sufficiently secure internet-connected devices and equipment across their entire lifecycles. To put some rather eye-opening numbers to it: a recent Ponemon Institute survey revealed that more than …

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CDRH Launches Pilot Program To Reduce Device Approval Times

CDRH Launches Pilot Program To Reduce Device Approval Times     The FDA Center for Devices and Radiological Health (CDRH) is launching the Total Product Life Cycle (TPLC) Advisory Program (TAP) Pilot. “TAP is a voluntary program intended to de-risk the medical device valley of death by providing industry with earlier and more frequent interactions with …

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