42 CFR 11.20
§ 11.20 Who must submit clinical trial registration information?
United States · 42 CFR — Public Health · Status: effective
Cite this
- Citation
- 42 CFR 11.20, § 11.20 Who must submit clinical trial registration information?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/200537
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Full text
The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.