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

  • ACMG Comments on FDA Plausible Mechanism Draft Guidance

  • Stakeholder Letter Opposing the Patent Eligibility Restoration Act (PERA)

  • Sign-on Letter to Evicore Regarding Interpretation of NCCN Guidelines

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

  • ACMG Response to Senate HELP Committee RFI on Diagnostics Regulation

  • Sign-on Letter Opposing the Patent Eligibility Restoraction Act of 2024

  • 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

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