21 CFR 1.715
§ 1.715 When must a user fee required by this subpart be submitted?
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 1.715, § 1.715 When must a user fee required by this subpart be submitted?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/82875
- Permanent ID
ys:prov:82875@1- SHA-256
c592c1e6e901e3cc65121ea0372c3bbc46f65e58c76461e722a36b918a5318d8
The hash is SHA-256 of this version's text, with every run of whitespace collapsed to a single space and the ends trimmed. The ID always leads back here, and checking it says whether the text you cited is still the current version.
Full text
(a) Accreditation bodies applying for recognition and third-party certification bodies applying for direct accreditation must submit a fee concurrently with submitting an application or a renewal application.
(b) Accreditation bodies and third-party certification bodies subject to an annual fee must submit payment within 30 days of receiving billing for the fee.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.