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BioWorld - Thursday, December 18, 2025
Home » Authors » Mark McCarty

Articles by Mark McCarty

Washington roundup: FDA: industry not the cause of CT overexposure incidents

Nov. 11, 2010
By Mark McCarty

Reimbursement 101: evidence for devices is often still lacking

Nov. 10, 2010
By Mark McCarty
WASHINGTON – The first day of the 2010 MDMA reimbursement seminar, sponsored by the Medical Device Manufacturers Association (MDMA; Washington), included a session dealing with reimbursement basics, but during her presentation on the subject, Judy Rosenbloom of JR Associates (Los Angeles), indicated that the reason she still offers a talk on the basics is that a lot of device makers still don't get the basics. (Medical Device Daily)
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Consultant: ACOs will march in time with the CE drumbeat

Nov. 10, 2010
By Mark McCarty

Washington roundup: TGA considers reclassifying ortho devices from IIb to III

Nov. 9, 2010
By Mark McCarty

Washington roundup: Shuren: CDRH eying special track for innovative devices

Nov. 8, 2010
By Mark McCarty

Washington roundup: FDA publishes long-awaited 510(k) guidance for FFDM

Nov. 5, 2010
By Mark McCarty

Washington roundup: CMS flouts Congress, MedPAC with 2011 fee schedule for ASCs

Nov. 4, 2010
By Mark McCarty

Washington roundup: Washington Legal Foundation tackles FDA re: Park doctrine

Nov. 3, 2010
By Mark McCarty

Washington roundup: Japan, UK agree to share info on drugs and devices

Nov. 2, 2010
By Mark McCarty

Shuren: user fee schedule affected by 510(k) review

Nov. 1, 2010
By Mark McCarty
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