10 CFR 35.2630: Records of dosimetry equipment used with remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.
Where this section sits in the code
- Title 10—Energy
- CHAPTER I—NUCLEAR REGULATORY COMMISSION
- PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
- Subpart L—Records
(a) A licensee shall retain a record of the calibration, intercomparison, and comparisons of its dosimetry equipment done in accordance with § 35.630 for the duration of the license.
(b) For each calibration, intercomparison, or comparison, the record must include—
(1) The date;
(2) The manufacturer's name, model numbers and serial numbers of the instruments that were calibrated, intercompared, or compared as required by paragraphs (a) and (b) of § 35.630;
(3) The correction factor that was determined from the calibration or comparison or the apparent correction factor that was determined from an intercomparison; and
(4) The names of the individuals who performed the calibration, intercomparison, or comparison.
Collected 2026-08-27T02:24:09Z. Source file · JSON