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Federal regulations · Through 2026-08-25 · Newer source version available

10 CFR 35.2630: Records of dosimetry equipment used with remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.

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Where this section sits in the code
  1. Title 10—Energy
  2. CHAPTER I—NUCLEAR REGULATORY COMMISSION
  3. PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
  4. 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

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