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What to Watch Between Now and July FDA event materials (briefing documents and background packets posted shortly before the meeting) Any FDA statements on enforcement discretion related to Category updates or interim policy API supply announcements from legitimate manufacturers moving into peptide production Provider marketing shifts (more compliance language, fewer miracle claims) as enforcement risk becomes clearer What This Means for Patients (and How to Reduce Risk) Patients dont control federal rulemaking, but you do control your risk profile

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and Behnood Bikdeli, MD, MS , Cardiovascular Medicine Division and the Thrombosis Research Group, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, and the YNHH/Yale Center for Outcomes Research and Evaluation (CORE), New Haven, CT, and the Cardiovascular Research Foundation, New York, NY