FDA Notice: Comment Request on Dietary Supplement CGMP Information Collection
A US Federal Register notice from the FDA announces a 60-day public comment period on the proposed collection of information under its current good manufacturing practice regulations for dietary supplements. It is a notice, not a final rule, and does not determine compliance or current law. [1]
Automatic summary · not editorially reviewed
The key findings
The source at a glance
- Jurisdiction
- US
- Authority
- Health and Human Services Department; Food and Drug Administration
- Document type
- Notice
- Record type / format
- Notice (Federal Register document record)
- Scope / context
- Dietary supplement manufacturers and other parties affected by FDA CGMP information collection provisions; public commenters.
- Summary based on
- Official regulatory document
- Original publication
- February 24, 2026
FDA notice on dietary supplement CGMP comment period
This is a notice from the US Department of Health and Human Services, Food and Drug Administration, published in the Federal Register on 2026-02-24. The agency announces an opportunity for public comment on a proposed collection of information. Under the Paperwork Reduction Act of 1995, federal agencies must publish notice of each proposed collection, including extensions of an existing collection, and allow 60 days for public comment. This notice solicits comments on the information collection provisions of FDA regulations on current good manufacturing practice for dietary supplements.
Supporting source [1]
What the notice covers and what it does not
The supplied text covers only the comment request on the information collection provisions of the dietary supplement CGMP regulations. It does not state the specific information being collected, the estimated burden, or any rule changes. The agency abstract notes that a proposed rule or notice is not a final rule, and that a publication date is not necessarily an effective date. The source alone does not determine a product's compliance or current legal status.
Supporting source [1]
Informational web rendition versus official legal edition
The web/API rendition is described as an informational resource, not the official legal edition. Readers are directed to verify the linked official PDF on GovInfo and applicable later amendments before relying on legal requirements. This is a document record, not a determination of current law, and it is not legal advice.
Supporting source [1]
How to interpret this
Document summary; not a determination of current law. Based only on the agency abstract and metadata; the full document was not reviewed. A notice is not a final rule, and a publication date is not necessarily an effective date.
Based on the cited official document. Its jurisdiction, document type and effective date matter; a proposal or notice is not a rule already in force.
Source & supporting passages
Health and Human Services Department; Food and Drug Administration · federalregister.gov · February 24, 2026