Public Policy Letters, Statements, Legal Briefs, & Other Responses
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ACMG Responds to FDA’s Approval for DTC Testing for Three BRCA Gene Mutations
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ACMG Letter Regarding South Carolina House Bill 3751 (2017) – Requesting Amendments
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ACMG Letter Regarding South Carolina Senate Bill 264 (2017) – Requesting Amendments
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ACMG/AMP/IDSA Joint Congressional Briefing on LDTs
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ACMG-AMP Joint Webinar on Regulatory Oversite of LDTs (recording)
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ACMG-AMP Joint Webinar on Regulatory Oversite of LDTs (slides)
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ACMG Response to Expansion of Direct-to-Consumer Genetic Testing
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ACMG One-Pager on FDA’s Proposed Regulatory Framework for LDTs
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Group Sign-on Letter to Congress Urging Modernization of the Clinical Laboratory Improvement Amendments (CLIA)
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ACMG Response to FDA’s Proposed Regulatory Framework for LDTs