Eli Lilly ·
Eli Lilly's litigation and public policy positions distinguish between legitimate 503A patient-specific compounding and what the company characterizes as 'mass compounding' that functions as drug manufacturing without approval. Lilly has not, as a matter of stated policy, opposed all compounding; its critiques have focused on scale, sourcing, and marketing. In court filings Lilly has repeatedly argued that the 503A framework presumes individualized prescribing by a clinician who has examined the patient, and that assembly-line compounding behind a telehealth questionnaire fails to meet that statutory requirement. This framing has influenced both judicial rulings and legislative proposals.
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