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

> Federal · Regulations · In force

URL: https://www.frixlaw.com/law-library/statutes/ecfr-42-11.6

## Section

- **Citation:** 42 CFR § 11.6
- **Heading:** What are the requirements for the submission of truthful information?
- **Jurisdiction:** Federal
- **Kind:** Regulations
- **Status:** In force
- **Text as of:** September 22, 2026
- **Source:** Publisher's official text
- **Location:** 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

## Text

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.

## Nearby sections

- [42 CFR § 11.2 § 11.2 What is the purpose of this part?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.2.md)
- [42 CFR § 11.4 § 11.4 To whom does this part apply?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.4.md)
- [42 CFR § 11.6 § 11.6 What are the requirements for the submission of truthful information?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.6.md)
- [42 CFR § 11.8 § 11.8 In what format must clinical trial information be submitted?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.8.md)
- [42 CFR § 11.10 § 11.10 What definitions apply to this part?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.10.md)
- [42 CFR § 11.20 § 11.20 Who must submit clinical trial registration information?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.20.md)
- [42 CFR § 11.22 § 11.22 Which applicable clinical trials must be registered?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.22.md)
- [42 CFR § 11.24 § 11.24 When must clinical trial registration information be submitted?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.24.md)
- [42 CFR § 11.28 § 11.28 What constitutes clinical trial registration information?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.28.md)
- [42 CFR § 11.35 § 11.35 By when will the NIH Director post clinical trial registration information submitted under § 11.28?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.35.md)
- [42 CFR § 11.40 § 11.40 Who must submit clinical trial results information?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.40.md)
- [42 CFR § 11.42 § 11.42 For which applicable clinical trials must clinical trial results information be submitted?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.42.md)
- [42 CFR § 11.44 § 11.44 When must clinical trial results information be submitted for applicable clinical trials subject to § 11.42?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.44.md)
- [42 CFR § 11.48 § 11.48 What constitutes clinical trial results information?](https://www.frixlaw.com/law-library/statutes/ecfr-42-11.48.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/ecfr-42-11.6. Check the current official text before relying on it. Not legal advice.