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BioWorld - Wednesday, January 14, 2026
Home » Authors » Mark McCarty

Articles by Mark McCarty

Washington roundup: Stanford v. Roche a warning to universities about contracts

June 9, 2011
By Mark McCarty

Washington roundup: ReGen docs say firm expressed 'disdain' for FDA review process

June 2, 2011
By Mark McCarty

Doc fix awaiting another patch

June 1, 2011
By Mark McCarty
Now that the U.S. House of Representatives has voted down a higher debt ceiling for the U.S. government, Congress can go back the drawing board on deciding how many Medicare spending cuts the voters and stakeholders can stomach, but as always, there are pockets of concern within the larger picture. The picture for device makers is somewhat complicated in part because the Medicare Part B “doc fix” is a $30 billion-a-year overhang that will be tough to resolve, not just because of the positions taken up on each side of Capitol Hill. On the Senate side, Kent Conrad (D-North...
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Washington roundup: Pitts, Pallone urge MedPAC to rethink Part B imaging data

June 1, 2011
By Mark McCarty

Washington roundup: FDA database for inspection classifications now available

May 30, 2011
By Mark McCarty

Washington roundup: CAPA cited as most common hit in device warning letters

May 27, 2011
By Mark McCarty

NIH spending take two

May 26, 2011
By Mark McCarty
A second look at NIH spending priorities By MARK McCARTY Medical Device Daily Washington Editor A couple of weeks ago, I posted something to this blog about NIH spending and whether it made sense, but there are other ways of doing the accounting. As I mentioned on May 1, the amount said to be allocated for the National Cancer Institute for fiscal 2010 was slightly more than $5 billion whereas the National Heart, Lung and Blood Institute took in about $2 billion less. This stands in contrast to the respective burdens of these disease groups, which is roughly $475 billion...
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Washington roundup: Congress passes bill to fund SBIR, STTR for another year

May 26, 2011
By Mark McCarty

FDA, devices and doom and gloom

May 25, 2011
By Mark McCarty
Is the sky falling? Device makers keep saying so By MARK McCARTY Medical Device Daily Washington Editor FDA's Center for Devices and Radiological Health is certainly on a regulatory tear of late, and industry is understandably rattled by some of the developments. After all, CDRH only recently managed to shed a couple of obvious malcontents in the persons of Robert Smith, MD, and Julian Nichols, MD, who both worked at the Office of Device Evaluation at CDRH and were not exactly happy to get their walking papers. My impression is that you have to be either really obnoxious, noticeably incompetent,...
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Washington roundup: Hutt tells Shuren guidance is 'terrific,' not followed at ODE

May 25, 2011
By Mark McCarty
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