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

  • 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 Opposing Updated VALID Act & ACM Exemption

  • Sign-on Letter to Congressional Leadership Concerning the VALID Act

  • ACMG Comments on FDA Draft Guidance for Products Incorporating Genome Editing

  • Group Sign-on Letter Concerning the VALID Act of 2022 Discussion Draft

  • ACMG Response to Opposing Inclusion of the VALID Act in the FDASLA Act

  • ACMG Letter to Michigan Medicaid on Coverage of Prenatal & Carrier Screening

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