{"data":{"id":"us/21-cfr-111.103","jurisdiction":"us","citation":"21 CFR 111.103","heading":"What are the requirements under this subpart F for written procedures?","body":"You must establish and follow written procedures for the responsibilities of the quality control operations, including written procedures for conducting a material review and making a disposition decision, and for approving or rejecting any reprocessing.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION","PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS","Subpart F—Production and Process Control System: Requirements for Quality Control"],"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":"94126a6cdce7ce8279db24124cf751a4a83fc273e1e2084ee969d0cdcd5248cc","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.95","next":"us/21-cfr-111.105"},"notice":"GroundRules: Original legal text. Not legal advice."}