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§ 11.20 Who must submit clinical trial registration information?

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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 B—Registration

This text was captured on Sep 22, 2026. It is a snapshot, not a live feed, so check the official code before relying on it.

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

This is a copy of a public record, reproduced as it was published. It is not legal advice, and it may not be the version a court would rely on. Check the official source before you cite it.

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