42 CFR 11.6: What are the requirements for the submission of truthful information?
Where this section sits in the code
- Title 42—Public Health
- CHAPTER I—PUBLIC HEALTH SERVICE, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER A—GENERAL PROVISIONS
- PART 11—CLINICAL TRIALS REGISTRATION AND RESULTS INFORMATION SUBMISSION
- Subpart A—General Provisions
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.
Collected 2026-08-27T02:26:11Z. Source file · JSON