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Demand continues to grow despite ongoing questions about: Human clinical trials Evidence of efficacy Appropriate dosing Long-term safety Product quality Compounding standards Supply-chain integrity For providers, the meeting may offer clues about how regulators view these challenges and whether future guidance could affect access to compounded peptide therapies

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We anticipated that this proposed informational-only feedback period will drive performance improvement for MIPS eligible clinicians, while continuing to support the statutory requirement for clinicians to be scored on cost as part of their composite performance score, as specified under section 1848(q)(5)(A) of the Act