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| Scientific Subdivisions | The Journal of Molecular Diagnostics | Contact AMP | |||||||||||
AMP, through its member leaders and its staff, advocates for the profession of molecular pathology and for the ability of its diverse membership to best serve patients. AMP is active in the legislative, regulatory, and reimbursement arenas.
The testimony of AMP President, Dr. Karen Mann, to the U.S. House of Representatives Committee on Science & Technology regarding the need for standard reference materials is featured on their website. Dr. Mann also presented these needs on June 9, by invitation, to the National Institute of Standards & Technology (NIST) Visiting Committee on Advanced Technology. The comments were prepared by AMP’s Clinical Practice Committee.
At their public meeting July 19-20, AMP cautioned FDA regarding unintended consequences, including the potential loss of ability to provide innovative tests, loss of ability to respond rapidly to emerging health threats, and potential discontinuation of needed services to patients. Comments were prepared by AMP's Professional Relations Committee.