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

  • ACMG Comments on FDA Plausible Mechanism Draft Guidance

  • Stakeholder Letter Supporting Joint Resolutions to Overturn FDA Rule on LDTs

  • ACMG Response to Senate HELP Committee RFI on Diagnostics Regulation

  • ACMG Response to RFI on Gene Therapies Access for Rare Diseases

  • ACMG Comments on FDA Proposed Rule for Regulation of LDTs

  • Stakeholder Letter Asking Congress Renew Efforts on CLIA Reform and Urge FDA to Halt LDT Rulemaking

  • Letter to FDA Requesting Extension of Comment Period for Proposed Rule on Regulation of LDTs

  • ACMG Request to FDA to Extend Comment Period for Proposed Rule on Regulation of LDTs

  • Sign-on Letter Supporting the Saving Access to Laboratory Services Act

  • ACMG Comment to NCD on Germline Editing and Impact on People with Disabilities

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