{"data":{"id":"us/21-cfr-211.3","jurisdiction":"us","citation":"21 CFR 211.3","heading":"Definitions.","body":"The definitions set forth in § 210.3 of this chapter apply in this part.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS","Subpart A—General Provisions"],"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":"d6de0c80472f7f44300f69ad40b892b5cc57c705c25e1a73934a0f3c8e728de4","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-211.1","next":"us/21-cfr-211.22"},"notice":"GroundRules: Original legal text. Not legal advice."}