HOUSE BILL 346 2025

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House Bill 346, known as the 'Access to Pediatric Rare Disease Treatment Information Act,' aims to amend Tennessee law regarding the management and sharing of essential treatment information for children diagnosed with rare diseases, particularly various forms of cancer. The bill establishes definitions, participation obligations for institutions, and procedures for maintaining and sharing treatment information among participating institutions. It also outlines the formation of an advisory board to provide guidance on implementation and ensure compliance with federal and state laws regarding patient privacy.

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HOUSE BILL 346 2025

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