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

42 CFR 11.20: Who must submit clinical trial registration 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 B—Registration

The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.

Collected 2026-08-27T02:26:11Z. Source file · JSON

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