The "Clinical Evaluation of Medical Device Software and Software as a Medical Device Training Course" training has been added to ResearchAndMarkets.com's offering. This course will provide a clear ...
The pharmaceutical and medical device industries stand at an inflection point. After decades of reliance on traditional randomized controlled trials (RCTs), computational modeling and simulation (CM&S ...
FDA uses a range of biocompatibility test data to evaluate medical devices before clearing or approving them for marketing. The growing use of FDA-recognized consensus standards facilitates this ...
GlobalData on MSN
Differing device regulation between regions causes trial challenges
Medical Devices includes a session from a regulatory expert on how companies can align their research between regions.
GlobalData on MSN
FDA announces regulatory exemptions for ‘non-medical grade’ devices
FDA commissioner Marty Makary revealed at the 2026 CES trade show in Las Vegas that low-risk devices will face less ...
DoP calls for proposals to set up common facilities for medical device clusters: Gireesh Babu, New Delhi Monday, January 12, 2026, 08:00 Hrs [IST] The Department of Pharmaceutical ...
Enrollment milestone achieved ahead of schedule as Solaris DE drug-eluting continues to gather additional clinical ...
BOSTON, MA, UNITED STATES, January 8, 2026 /EINPresswire.com/ -- EyeCool Therapeutics, a clinical-stage ophthalmic ...
Dublin, July 30, 2025 (GLOBE NEWSWIRE) -- The "Clinical Evaluation of Medical Device Software and Software as a Medical Device Training Course" training has been added to ResearchAndMarkets.com's ...
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