|Scientific Subdivisions | The Journal of Molecular Diagnostics
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October 15, 2015: Brian J. Druker, MD, Director, Knight Cancer Institute will receive this year's AMP Award for Excellence. Congratulations to Dr. Druker and to AMP members Barbara A. Zehnbauer, PhD, and Roger D. Klein, MD, JD, for earning the Jeffrey A. Kant Leadership Award and the AMP Meritorious Service Award, respectively. They and other award winners will be honored at AMP 2015, November 5-7 in Austin, TX.
This month's issue is full of updates on AMP advocacy and educational initiatives as well as Annual Meeting highlights and innovative endeavors.
October 1, 2015: AMP article in the November issue of The Journal of Molecular Diagnostics, reviews NGS applications, challenges, and opportunities in infectious disease testing. "NGS holds enormous promise for clinical infectious diseases testing," said Benjamin Pinsky, MD, corresponding author.
August 4, 2015: Proposal provides assurance of quality, analytical validity, and clinical validity without jeopardizing innovation or patient access to necessary care in a tiered, risk-based structure that avoids duplication of activities within and between federal agencies.
June 4, 2015: The article, published in The Journal of Molecular Diagnostics, describes the current and future roles of the laboratory professional as genomic sequencing analysis becomes an ever more increasingly important tool in diagnostic medicine.
May 21, 2015: The AMP Board of Directors voted unanimously to launch an International Affairs Committee (IAC). The IAC stems from the International Affairs Working Group which, since 2010, has launched numerous successful education and collaboration opportunities with professionals and organizations outside the U.S.
April 20, 2015: May 2015 issue of JMD includes AMP article indicating that minimally invasive diagnostic techniques for cancer detection are promising and provide hope for enhanced patient care.
March 30, 2015: ASCP, CAP, AMP, and ASCO issued a draft of a colorectal cancer molecular marker testing guideline and announced the opening of a public comment period The evidence-based guideline will help establish standard molecular marker testing, guide targeted therapies, and advance personalized care for these patients. More Information...
March 20, 2015: AMP's feedback urges FDA to focus its attention on helping to ensure the performance characteristics of NGS instruments, reagents, and related software.
March 4, 2015: These models are available for free and can be used to effectively communicate the cost and value of genomic sequencing procedure services to Medicare and commerical payers.
February 20, 2015: In its verbal comments to the FDA, AMP recommends FDA focus on evaluating and ensuring consistent performance of NGS diagnostic tests.
February 12, 2015: AMP Working Group recommends that laboratories develop individual policies for analysis and reporting of known and predicted incidental findings.
February 12, 2015: AMP and CAP signed a memorandum of understanding to foster synergies between the sub-specialty of molecular pathology and the general practice of pathology.
February 10, 2015: Updated position on Direct Access Genetic testing, concludes that clinically meaningful tests could benefit patients and consumers and should be made to the public, but only if certain conditions are met.
January 29, 2015: AMP expresses numerous concerns with FDA's proposed draft framework including its interference with the practice of medicine and its potential impact on patient access to vital molecular testing services that AMP members and their laboratories offer.
January 12, 2015: CAP, IASLC, and AMP have teamed up to revise the evidence-based guideline, "Molecular Testing Guideline for Selection of Lung Cancer Patients for EGFR and ALK Tyrosine Kinase Inhibitors."
January 8, 2015: White Paper addresses the convergence of regulatory and reimbursement forces that threaten patient care. "AMP is addressing the consequences of this gathering perfect storm of regulatory and reimbursement challenges directed against molecular diagnostic testing with recommendations designed to preserve patient access to these essential medical services" said AMP President, Janina Longtine, MD.Â More information...
January 8, 2015: FDA's Public Workshop - Framework for Regulatory Oversight of LDTs, includes presentations by ten AMP members. Message emphasizes optimization of patient care through molecular diagnostics.
January 5, 2015: AMP responded to specific questions posed by the U.S. Energy and Commerce Committee regarding LDPs and spelled out clear recommendations for ensuring patient care.