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BioWorld - Sunday, December 14, 2025
Home » Authors » Mark McCarty

Articles by Mark McCarty

Washington roundup: GAO says Medicare needs more pre-auth, better pay-and-chase

June 21, 2010
By Mark McCarty

Washington roundup: Optovue files 510(k) to deal with software after warning

June 18, 2010
By Mark McCarty

Washington roundup: Artegraft warning letter cites sterilization, process changes

June 17, 2010
By Mark McCarty

IOM hears from all sides in ongoing debate over 510(k)s

June 16, 2010
By Mark McCarty

Washington roundup: FDA discussed genetic tests with Dx firms in August '09

June 15, 2010
By Mark McCarty

AAPM; clinics responsible for QA, but industry must pitch in

June 14, 2010
By Mark McCarty

Clinical community arguing for more stringent standards

June 11, 2010
By Mark McCarty
GAITHERSBURG, Maryland – The first of the two-day meeting on dosing for radiotherapeutic equipment covered a fair amount of ground, but one message was resonant on the part of providers. The message was not explicitly that there is no such thing as a safe radiotherapeutic device on the market at the moment, but representatives of the clinical community seemed disinclined to believe that the current generation of radiotherapeutic devices is adequately equipped to do a reasonable job of providing a "reasonable assurance of safety and efficacy," as the saying goes. (Medical Device Daily)
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Washington roundup: FDA inks warning letter to Otologics for documentation

June 9, 2010
By Mark McCarty

Washington roundup: Endocare hit for failure to file MDR for patient death

June 4, 2010
By Mark McCarty

Washington roundup: Dexcom: FDA flip-flopped on wire fracture device reports

June 3, 2010
By Mark McCarty
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