{"data":{"id":"us/21-cfr-320.1","jurisdiction":"us","citation":"21 CFR 320.1","heading":"Definitions.","body":"The definitions contained in § 314.3 of this chapter apply to those terms when used in this part.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER D—DRUGS FOR HUMAN USE","PART 320—BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS","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":"2f8aa1314d2346be8245af7b30a4d87c9c656d23c19dcf24bfc931463af6b9a5","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-317.2","next":"us/21-cfr-320.21"},"notice":"GroundRules: Original legal text. Not legal advice."}