What does MDUFMA stand for?

Medical Device User Fee and Modernization Act

This definition appears very rarely and is found in the following Acronym Finder categories:

Military and Government
Science, medicine, engineering, etc.

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Samples in periodicals archive:

They developed the Office of Combined Products (OCP) which was a result of the Medical Device User Fee and Modernization Act of 2002 (MDUFMA).

FDA Resolves Compliance Issues with Drug/Device Combination Products

GAO inspectors found that while a third-party program was established by the Medical Device User Fee and Modernization Act of 2002 to assist with inspections of foreign facilities, the FDA accredited only two third parties and completed only four inspections between March 2004 and May 2008.

FDA faulted for oversight of foreign medical device and drug makers

Fees were first put in place by the Medical Device User Fee and Modernization Act of 2002 (23) (MDUFMA).

Cost recovery and the future of the medical device regulation program ...

FDA April 16 proposed recommendations to Congress for reauthorizing the Medical Device User Fee and Modernization Act (MDUFMA II), which, if adopted, "would help to ensure that safe and effective medical devices get to patients in a timely manner," the agency said in a statement.

FDA announces recommendations to reauthorize MDUFMA

The Food and Drug Administration floated the increase as part of its recommendations to Congress for reauthorizing the Medical Device User Fee and Modernization Act.

Medical device firms to pay more

The Food and Drug Administration floated the increase as part of its recommendations to Congress for reauthorizing the Medical Device User Fee and Modernization Act.

FDA proposes exacting more in fees from medical device companies

Market Updates Senate offers plan on FDA user fees A Senate committee last month took a step forward in addressing the rising costs associated with the Medical Device User Fee and Modernization Act (MDUFMA), which have been a concern to device companies especially of the early-stage variety and industry organizations.

Market Updates

The new edition of this popular and authoritative resource addresses the latest regulatory and legal developments that guide how medical devices are developed today: * The Medical Device User Fee and Modernization Act of 2002, including user fees, third party inspections, reprocessed single use devices, and the establishment of the Office of Combination Products.

Research and Markets: Medical Device Development: Regulation and Law, ...