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diagnostic testing should only be done by healthcare professionals in a clinical setting.) Administration Details: Sermorelin is supplied as a lyophilized powder in sterile vials that require reconstitution with the provided diluent (usually bacteriostatic water for injection)

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Our clinical staff is trained to monitor patients closely during and after the procedure for any signs of an adverse reaction

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It is scheduled for review by the FDA Pharmacy Compounding Advisory Committee (PCAC) on July 23, 2026, as a substance nominated for possible inclusion on that list

The absence of clinical guidelines leaves surgeons navigating an evidence gap with potential medicolegal implications, particularly when patients undergo elective procedures where the acceptable tolerance for unmeasured risk is low