{"data":{"id":"us/42-cfr-11.20","jurisdiction":"us","citation":"42 CFR 11.20","heading":"Who must submit clinical trial registration information?","body":"The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.","path":["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"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-42.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:26:11Z","sha256":"0a3acb67f3f672c7ee0159b86373ed5d2c6bd6f1d217605dc4175bdc433252b3","source_id":"us-cfr","stale":true,"prev":"us/42-cfr-11.10","next":"us/42-cfr-11.22"},"notice":"GroundRules: Original legal text. Not legal advice."}