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The Better Care for PFAS Patients Act requires the Director of the Agency for Toxic Substances and Disease Registry to contract with the National Academies of Sciences, Engineering, and Medicine (or another entity) to periodically assess the health effects of per- and polyfluoroalkyl substances (PFAS) and formulate clinical recommendations. The Director must issue updated clinical guidance based on these assessments at least every 5 years, post it on the agency's public website, and disseminate it to state and local health authorities and healthcare professionals. The initial assessment and recommendations must be completed within 2 years of the agreement, with updates occurring more frequently if warranted by new scientific evidence.
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