FDA / Federal Register Notice: Agency Information Collection Activities; Proposed Collection; Comment Request; Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act
FDA seeks comments on human drug compounding practices.
What changed & why it matters
Med Spa Radar recorded a Federal Register notice at the federal level, dated November 24, 2025, in the GLP-1 Compounding category.
Federal Register activity is where federal compounding policy is actually written — proposed rules, comment periods, and clinical-need determinations that decide which bulk substances may be compounded under sections 503A and 503B.
- Type
- Federal Register
- Jurisdiction
- Federal
- Category
- GLP-1 Compounding
- Recorded
- November 24, 2025
What this means for your specific practice — the exact step to take, the deadline to calendar, or the supplier detail to check — is in the member "what to do" below. This page is the free record of what changed and why it matters.
What to do
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Federal Register · primary source ↗
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Monitoring, not legal advice.