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Federal regulations · Through 2026-08-25 · Newer source version available

42 CFR 11.6: What are the requirements for the submission of truthful information?

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Where this section sits in the code
  1. Title 42—Public Health
  2. CHAPTER I—PUBLIC HEALTH SERVICE, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  3. SUBCHAPTER A—GENERAL PROVISIONS
  4. PART 11—CLINICAL TRIALS REGISTRATION AND RESULTS INFORMATION SUBMISSION
  5. 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

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