{"data":{"id":"us/21-cfr-230.70","jurisdiction":"us","citation":"21 CFR 230.70","heading":"Supplements and other changes to a granted certification.","body":"(a) The applicant must submit a supplement if any information in the certification request changes after the request has been deemed granted, including, but not limited to, the addition of a new facility manufacturing the designated medical gas, a change in contact information, or a change in the corporate name.\n(b) Each supplement must include a signed, completed request for certification form with the updated information in accordance with § 230.50. The updated information must be submitted no later than 30 calendar days after the date the change occurred.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 230—CERTIFICATION AND POSTMARKETING REPORTING FOR DESIGNATED MEDICAL GASES","Subpart B—Certification of Designated Medical Gases"],"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":"105d4b8010edcb80162967299d4793203f1247f4b05ec4e52696b76fdd6d6e11","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-230.65","next":"us/21-cfr-230.72"},"notice":"GroundRules: Original legal text. Not legal advice."}