StacksVerified U.S. regulatory reference

42 CFR §11.6

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
The clinical trial information submitted by a responsible party under this part shall not be false or misleading in any particular. A responsible party who submits false and/or misleading information is subject to civil monetary penalties and/or other civil or criminal remedies available under U.S. law.