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42 CFR 11.40

§ 11.40 Who must submit clinical trial results information?

United States · 42 CFR — Public Health · Status: effective

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42 CFR 11.40, § 11.40 Who must submit clinical trial results information?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/200543
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The responsible party for an applicable clinical trial specified in § 11.42 must submit clinical trial results 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.