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Regulations last checked for updates: May 06, 2024
Title 10 - Energy last revised: May 01, 2024
All Titles
Title 10
Chapter I
Part 35 - PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
Subpart A [§ 35.1 - § 35.19] - Subpart A—General Information
Subpart B [§ 35.24 - § 35.59] - Subpart B—General Administrative Requirements
Subpart C [§ 35.60 - § 35.92] - Subpart C—General Technical Requirements
Subpart D [§ 35.100 - § 35.290] - Subpart D—Unsealed Byproduct Material—Written Directive Not Required
Subpart E [§ 35.300 - § 35.396] - Subpart E—Unsealed Byproduct Material—Written Directive Required
Subpart F [§ 35.400 - § 35.491] - Subpart F—Manual Brachytherapy
Subpart G [§ 35.500 - § 35.590] - Subpart G—Sealed Sources for Diagnosis
Subpart H [§ 35.600 - § 35.690] - Subpart H—Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units
Subpart I - Subparts I-J [Reserved]
Subpart K [§ 35.1000 - § 35.1000] - Subpart K—Other Medical Uses of Byproduct Material or Radiation From Byproduct Material
Subpart L [§ 35.2024 - § 35.2655] - Subpart L—Records
Subpart M [§ 35.3045 - § 35.3204] - Subpart M—Reports
Subpart N [§ 35.4001 - § 35.4002] - Subpart N—Enforcement
authority:
Atomic Energy Act of 1954, secs. 81, 161, 181, 182, 183, 223, 234, 274 (
42 U.S.C. 2111
,
2201
,
2231
,
2232
,
2233
,
2273
,
2282
,
2021
; Energy Reorganization Act of 1974, secs. 201, 206 (
42 U.S.C. 5841
,
5846
;
44 U.S.C. 3504
note
source:
67 FR 20370, Apr. 24, 2002, unless otherwise noted.
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