{"data":{"id":"us/21-cfr-812.45","jurisdiction":"us","citation":"21 CFR 812.45","heading":"Informing investigators.","body":"A sponsor shall supply all investigators participating in the investigation with copies of the investigational plan and the report of prior investigations of the device.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 812—INVESTIGATIONAL DEVICE EXEMPTIONS","Subpart C—Responsibilities of Sponsors"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"b3dc115484fa1b0792b200735b377d2237b50b696d0ba19883c4dbc99447d05b","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-812.43","next":"us/21-cfr-812.46"},"notice":"GroundRules: Original legal text. Not legal advice."}