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)
- SUBPART I — J [Reserved]
- SUBPART K — Other Medical Uses of Byproduct Material or Radiation From Byproduct Material (§§ 35.1000 - 35.1000)
- SUBPART L — Records (§§ 35.2024 - 35.2655)
- SUBPART M — Reports (§§ 35.3045 - 35.3067)
- SUBPART N — Enforcement (§§ 35.4001 - 35.4002)
Authority:
Atomic Energy Act secs. 81, 161, 181, 182, 183, 223, 234 (42 U.S.C. 2111, 2201, 2231, 2232, 2233, 2273, 2282); Energy Reorganization Act sec. 201, 206 (42 U.S.C. 5841, 5842, 5846); sec. 1704 (44 U.S.C. 3504 note); Energy Policy Act of 2005, sec. 651(e), Pub. L. 109-58, 119 Stat. 806-810 (42 U.S.C. 2014, 2021, 2021b, 2111).
Source:
67 FR 20370, Apr. 24, 2002, unless otherwise noted.
Title 10 published on 2015-01-01.
No entries appear in the Federal Register after this date, for 10 CFR Part 35.