{"data":{"id":"us/10-cfr-35.406","jurisdiction":"us","citation":"10 CFR 35.406","heading":"Brachytherapy sources accountability.","body":"(a) A licensee shall maintain accountability at all times for all brachytherapy sources in storage or use.\n(b) As soon as possible after removing sources from a patient or a human research subject, a licensee shall return brachytherapy sources to a secure storage area.\n(c) A licensee shall maintain a record of the brachytherapy source accountability in accordance with § 35.2406.","path":["Title 10—Energy","CHAPTER I—NUCLEAR REGULATORY COMMISSION","PART 35—MEDICAL USE OF BYPRODUCT MATERIAL","Subpart F—Manual Brachytherapy"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-10.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:09Z","sha256":"6621bc7e8db163111bb546017fdcd91e98261c49a4baad8b45646eeaf6c2287c","source_id":"us-cfr","stale":true,"prev":"us/10-cfr-35.404","next":"us/10-cfr-35.410"},"notice":"GroundRules: Original legal text. Not legal advice."}