{"data":{"id":"us/21-cfr-226.10","jurisdiction":"us","citation":"21 CFR 226.10","heading":"Personnel.","body":"The key personnel and any consultants involved in the manufacture and control of the Type A medicated article(s) shall have a background of appropriate education or appropriate experience or combination thereof for assuming responsibility to assure that the Type A medicated article(s) has the proper labeling and the safety, identity, strength, quality, and purity that it purports to possess.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES","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":"2d8113f4800da6ed08d4a184712d5f70c437fe950e50827853e8022c2552d4f6","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-226.1","next":"us/21-cfr-226.20"},"notice":"GroundRules: Original legal text. Not legal advice."}