{"data":{"id":"us/42-cfr-11.40","jurisdiction":"us","citation":"42 CFR 11.40","heading":"Who must submit clinical trial results information?","body":"The responsible party for an applicable clinical trial specified in § 11.42 must submit clinical trial results 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 C—Results Information Submission"],"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":"6723c4d42dc5e2305b1b1e233602249926ce1ace975afaf658a9dfd429f865b6","source_id":"us-cfr","stale":true,"prev":"us/42-cfr-11.35","next":"us/42-cfr-11.42"},"notice":"GroundRules: Original legal text. Not legal advice."}
