{"data":{"id":"us/42-cfr-11.6","jurisdiction":"us","citation":"42 CFR 11.6","heading":"What are the requirements for the submission of truthful information?","body":"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.","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 A—General Provisions"],"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":"9881dc70007e272dc72752d67a1dcd3aedcc8e0a8e97e43da1fd0652156ed191","source_id":"us-cfr","stale":true,"prev":"us/42-cfr-11.4","next":"us/42-cfr-11.8"},"notice":"GroundRules: Original legal text. Not legal advice."}