10 CFR Part 35 - MEDICAL USE OF BYPRODUCT MATERIAL
- Subpart A—General Information (§§ 35.1 - 35.19)
- Subpart B—General Administrative Requirements (§§ 35.24 - 35.59)
- Subpart C—General Technical Requirements (§§ 35.60 - 35.92)
- Subpart D—Unsealed Byproduct Material—Written Directive Not Required (§§ 35.100 - 35.290)
- Subpart E—Unsealed Byproduct Material—Written Directive Required (§§ 35.300 - 35.396)
- Subpart F—Manual Brachytherapy (§§ 35.400 - 35.491)
- Subpart G—Sealed Sources for Diagnosis (§§ 35.500 - 35.590)
- Subpart H—Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units (§§ 35.600 - 35.690)
- Subparts I-J [Reserved]
- Subpart K—Other Medical Uses of Byproduct Material or Radiation From Byproduct Material (§ 35.1000)
- Subpart L—Records (§§ 35.2024 - 35.2655)
- Subpart M—Reports (§§ 35.3045 - 35.3204)
- Subpart N—Enforcement (§§ 35.4001 - 35.4002)
Authority:
Source:
67 FR 20370, Apr. 24, 2002, unless otherwise noted.
Editorial Note:
Nomenclature changes to part 35 appear at79 FR 75739, Dec. 19, 2014.