{"data":{"id":"us/21-cfr-640.125","jurisdiction":"us","citation":"21 CFR 640.125","heading":"Definitions.","body":"The definitions set out in § 630.3 of this chapter apply to the use of those defined terms in this part.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER F—BIOLOGICS","PART 640—ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS","Subpart M—Definitions and Medical Supervision"],"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":"d32fce2d57316779dddf0bf21020168c822985048e88535dfe4e797bb3ecf5f8","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-640.120","next":"us/21-cfr-640.130"},"notice":"GroundRules: Original legal text. Not legal advice."}