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ASM Attends UN General Assembly

ASM President, Susan Sharp, Ph.D., joined global leaders at the United Nations General Assembly in New York today in a historical meeting to focus on the commitment to fight AMR.
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UN General Assembly Focuses on AMR

Leaders at the UN General Assembly draft a plan for coordinated, cross-cutting efforts to improve the current state of AMR.
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Superbugs are a 'Fundamental Threat'

If antibiotics were telephones, we would still be calling each other using clunky rotary dials and copper lines," Stefano Bertuzzi, CEO of ASM, told NBC News.
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On January 30-31, 2002, ASM members Alice Weissfeld (CLIAC member), Patricia Charache (CLIAC member), and David Sewell attended the CLIAC meeting. The Food and Drug Administration (FDA), Centers for Medicare and Medicaid Services (CMS), Centers for Disease Control and Prevention (CDC), and CLIAC workgroups provided updates to the full committee.

FDA

The FDA has withdrawn its draft waiver guidance and the criteria for waiver as published in the 1995 proposed waiver rule would be used for evaluation of requests for waived status. CLIAC sent its comments on the proposed criteria for waiver to the Secretary of Health and Human Services (HHS). Dr. Cowan (FDA) presented a report on the Blood Products Advisory Committee session (6/14/01) addressing the applicability of waivers to HIV rapid tests. The FDA will update CLIAC when substantive progress is made.

CMS

The CLIAC members discussed the proposed rule for the qualification requirements for directors of laboratories performing high complexity testing and concluded that Alternative 3 in the proposed rule was vague. CLIAC recommended that a higher standard be required as provided by certification from a board approved by HHS.

CMS anticipates publication of proposed QC/QA guidelines in the Federal Register no later than December 2002.

CDC

CDC is hopeful that a Quality Institute (QI) can be established to provide a forum for defining quality laboratory systems. The QI would include representatives from all areas of healthcare. CLIAC supports the development of the QI and a National Laboratory System.

Genetic Testing

Dr. Charache updated CLIAC on the work accomplished by the Secretary's Advisory Committee on Genetic Testing (SACGT). Both SACGT and CLIAC provide advice to CDC and HHS on CLIA requirements for genetic testing.

In Vitro Devices (IVD) Regulations

Kay Setzer, a manufacturer's liaison representative on CLIAC, presented a concise overview of the regulatory process for FDA approval of IVDs.

Health Insurance Portability and Accountability Act (HIPAA)

CLIAC recommended that HHS carefully review the apparent requirement in HIPAA that CMS "deemed" organizations must set up a "business associate" relationship with all laboratories receiving accreditation inspection and proficiency testing material.

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