Public Policy Letters, Statements, Legal Briefs, & Other Responses

  • ACMG/AMP/IDSA Joint Congressional Briefing on LDTs

  • ACMG-AMP Joint Webinar on Regulatory Oversite of LDTs (slides)

  • ACMG-AMP Joint Webinar on Regulatory Oversite of LDTs (recording)

  • ACMG Comments to EEOC Concerning Proposed Rule Related to the Genetic Information Nondiscrimination Act (GINA)

  • ACMG Comments to OHRP Concerning Proposed Revisions to the Common Rule

  • ACMG Response to FDA’s Proposed Regulatory Framework for LDTs

  • ACMG One-Pager on FDA’s Proposed Regulatory Framework for LDTs

  • Group Sign-on Letter to Congress Urging Modernization of the Clinical Laboratory Improvement Amendments (CLIA)

  • ACMG Comments to EEOC Concerning Regulations Under the Americans with Disabilities Act (ADA)

  • ACMG Comments to FDA Concerning the FDA Draft Guidance on the Framework for Regulatory Oversight of LDTs

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