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BioWorld - Thursday, January 22, 2026
Home » Authors » Mark McCarty

Articles by Mark McCarty

Penumbra's handling of 070 catheter draws FDA warning

Jan. 14, 2010
By Mark McCarty

Washington roundup: FDA's transparency initiative gains toehold on the Internet

Jan. 13, 2010
By Mark McCarty

Washington roundup: Eshoo, Paulsen urge Pelosi to dial back medical device tax

Jan. 12, 2010
By Mark McCarty

Washington roundup: Associations see legislative prospects as mixed for 2010

Jan. 11, 2010
By Mark McCarty

Washington roundup: FDA writes MicroMed cryptic warning for event reporting

Jan. 7, 2010
By Mark McCarty

Long-term care issues revolve around ageless issue of cost

Jan. 6, 2010
By Mark McCarty

Washington roundup: ACC sues over SGR fee cuts to Medicare Part B payments

Dec. 31, 2009
By Mark McCarty

Washington roundup: JAMA: devices are subject to less scrutiny than drugs

Dec. 30, 2009
By Mark McCarty
The process of clearance and approval of medical devices has been all over the media radar screen, and the Journal of the American Medical Association (JAMA) has chimed in with an article alleging that device applications have been subjected to less scrutiny than drug applications. (Medical Device Daily)
Read More

Washington roundup: NICE indicates unwillingness to cover dronedarone for afib

Dec. 29, 2009
By Mark McCarty

Washington roundup: Senate's health reform bill faces merger with House bill

Dec. 28, 2009
By Mark McCarty
The U.S. Senate has pushed through a healthcare reform bill – a mammoth 2,500-page chunk of legislation with bargains grand and petite for a number of stakeholders – by a party-line vote of 60-39. Despite the seeming momentousness of the occasion, one last hurdle remains: managing the merger of the Senate's legislative tome with the relatively house bill, which comes in at roughly 1,100 pages. (Medical Device Daily)
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