
FAIR COMPOUNDING REGULATIONS
Regulation Should Protect Patients — Not Block Their Care
When regulators treat compounded medicine like commercial manufacturing, patients lose access to vital treatments they can’t get anywhere else.
503A compounding pharmacies are built to create patient-specific medications with physician oversight. But increasingly, the FDA and state boards are applying manufacturing-level restrictions designed for mass-market drug production — even when no commercial alternative exists.
This is regulatory overreach, not public safety.Who’s Being Harmed
Thousands of everyday prescriptions for patients with chronic conditions
Provider authority to prescribe customized therapies
Pharmacy access in underserved communities
Affordable alternatives when branded meds are cost-prohibitive
WHAT NEEDS TO CHANGE
We need clear distinction between manufacturers and compounders – and rules that reflect reality, not pressure from Big Pharma. Regulation must be based on science, not fear or politics.
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