Home/CFR/Title 42/Part 11/§ 11.8
42 CFR · Public Health

§ 11.8 — In what format must clinical trial information be submitted?

42 CFR § 11.8
TitleTitle 42: Public HealthPartPart 11: Clinical Trials Registration and Results Information Submission
SourceeCFR (current through Apr 6, 2026)

This text of 42 C.F.R. § 11.8 (In what format must clinical trial information be submitted?) is published on Counsel Stack Legal Research, covering United States primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
42 C.F.R. § 11.8 (2026).

Text

§ 11.8 In what format must clinical trial information be submitted? Information submitted under this part must be submitted electronically to ClinicalTrials.gov, in the format specified at https://clinicaltrials.gov or successor site. [81 FR 65138, Sept. 21, 2016, as amended at 89 FR 97559, Dec. 9, 2024]

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Nearby Sections

9
§ 11.2
What is the purpose of this part?
§ 11.4
To whom does this part apply?
§ 11.6
What are the requirements for the submission of truthful information?
§ 11.8
In what format must clinical trial information be submitted?
§ 11.10
What definitions apply to this part?
§ 11.20
Who must submit clinical trial registration information?
§ 11.22
Which applicable clinical trials must be registered?
§ 11.24
When must clinical trial registration information be submitted?
§ 11.28
What constitutes clinical trial registration information?

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Bluebook (online)
42 C.F.R. § 11.8, Counsel Stack Legal Research, https://law.counselstack.com/cfr/42/11/11.8.
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