42 C.F.R. § 11.6

What are the requirements for the submission of truthful information?

Last amended: 2017Year: 2026Length: 46 wordsOfficial source

Cite as 42 C.F.R. § 11.6 (2026)

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.
42 C.F.R. § 11.6: What are the requirements for the submission of truthful information? | Justis AI