10 CFR 35.60: Possession, use, and calibration of instruments used to measure the activity of unsealed byproduct material.
Where this section sits in the code
- Title 10—Energy
- CHAPTER I—NUCLEAR REGULATORY COMMISSION
- PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
- Subpart C—General Technical Requirements
(a) For direct measurements performed in accordance with § 35.63, a licensee shall possess and use instrumentation to measure the activity of unsealed byproduct material before it is administered to each patient or human research subject.
(b) A licensee shall calibrate the instrumentation required in paragraph (a) of this section in accordance with nationally recognized standards or the manufacturer's instructions.
(c) A licensee shall retain a record of each instrument calibration required by this section in accordance with § 35.2060.
Collected 2026-08-27T02:24:09Z. Source file · JSON