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Biopharma & Medical Device Briefing: PFAS Reporting Requirements; ECHA Substances of ...

Retrieved on: 2024-10-24 21:37:59

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The article discusses regulatory updates relevant to biopharma, highlighting the EPA's proposed delay for PFAS reporting, ECHA's proposed addition of chemicals to the SVHC list, and microRNA's discovery impacting gene regulation, aligning with the key concept and tags provided.

Article found on: www.jdsupra.com

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