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Alliance Celebrates the First-Ever, FDA approval of a Transcatheter Therapy for the Treatment of Tricuspid Regurgitation

Alliance Celebrates the First-Ever, FDA approval of a Transcatheter Therapy for the Treatment of Tricuspid Regurgitation
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Physician Expectations Regarding the FDA Approval Process May Differ From Reality

Sanket Dhruva, MD, MHS, details examining the perspectives of physicians regarding the FDA approval process for drugs and high-risk medical devices.

United statesHealth affairsBreakthrough devices programUniversity of california san franciscoInnovation actCalifornia san franciscoAmerican boardInternal medicineSanket dhruvaFda approval processPhysician expectationsA more rigorous fda approval processHigh risk medical devicesNovel agentsHealth affairs

FDA Grants Breakthrough Device Designation to Amadix´s preventive screening blood test for Colorectal Cancer

/PRNewswire/ Amadix, a Spanish biotech company, announced today that PreveCol®, its colorectal cancer screening blood test, has received Breakthrough Device.

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FDA Grants Breakthrough Device Designation to Amadix s preventive screening blood test for Colorectal Cancer

FDA Grants Breakthrough Device Designation to Amadix s preventive screening blood test for Colorectal Cancer
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Biomimetic Innovations Ltd: FDA grants global Medical Device company Biomimetic Innovations Breakthrough Device designation for OsStic® Synthetic Injectable Structural Bio-Adhesive Bone Void Filler

Biomimetic Innovations Ltd: FDA grants global Medical Device company Biomimetic Innovations Breakthrough Device designation for OsStic® Synthetic Injectable Structural Bio-Adhesive Bone Void Filler
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United statesStefan klotterPaul burkeBronagh odohertyThomasa russellBiomimetic innovations ltdBreakthrough devices programBreakthrough deviceSynthetic injectable bone void fillerBreakthrough designationInnovations ltdProduct managerDie performance strategieAssets sie