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

Articles by Mark McCarty

Tyler advising FDA to fill in statutory voids aggressively

April 23, 2010
By Mark McCarty
WASHINGTON – FDA Commissioner Margaret Hamburg, MD, opened the plenary session on the first day of the 53rd Annual FDLI Conference, hosted by the Food and Drug Law Institute (FDLI; Washington), and she made it clear at the outset that the agency will not hesitate to ask Congress for additional statutory authority should she conclude that such a request would be appropriate. On the other hand, the agency's new chief counsel, Ralph Tyler, also made a point very clear, that his office would do its best to facilitate enforcement action even in the absence of direct statutory authority, assuming that the intended action does not explicitly run afoul of the statute. (Medical Device Daily)
Read More

Washington roundup: FDA announces initiative for medical devices for home use

April 22, 2010
By Mark McCarty

Washington roundup: Clawbacks offset updates for long-term, acute care hospitals

April 21, 2010
By Mark McCarty

Washington roundup: AHRQ says infections acquired in hospitals are still an issue

April 19, 2010
By Mark McCarty

Washington roundup: Journal article says ICD use in older patients needs study

April 16, 2010
By Mark McCarty

Washington roundup: GE, Virginia Tech win patent for new CT angio technology

April 15, 2010
By Mark McCarty

Washington roundup: AAA surgery said as effective and cheaper than percutaneous

April 13, 2010
By Mark McCarty

Washington roundup: Software drives FDA's worries over radiotherapy equipment

April 12, 2010
By Mark McCarty

Washington roundup: FDA out of RAPS 510(k) talk, blog questions transparency

April 9, 2010
By Mark McCarty

Washington roundup: JAMA article lacks outcomes, but claims fusion is overused

April 8, 2010
By Mark McCarty
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