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Association for Molecular Pathology

AMP Archived News - 2016

AMP Responds to FDA Report on Ovesight of Laboratory Developed Testing Procedures

December 16, 2015: AMP analysis concludes report grossly misrepresents the public health concerns of laboratory developed testing procedures.
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AMP Submits Written Testiomy for Hearing on "Examining the Regulation of Diagnostic Tests and Laboratory Operations"

November 18, 2015: AMP has submitted written testimony to the House Energy and Commerce Subcommittee on Health for their hearing on "Examining the Regulation of Diagnostic Tests and Laboratory Operations." AMP urged the Committee to use AMP's proposal to modernize the Clinical Laboratory Improvement Amendments (CLIA) at the Centers for Medicare & Medicaid Services (CMS) as the basis for legislation that would preserve innovative patient care by building upon the current CMS-based system for oversight of laboratory developed procedures (LDPs).
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