PART 35—MEDICAL USE OF BYPRODUCT MATERIAL
- SUBPART A—General Information (§35.1 to §35.19)
- SUBPART B—General Administrative Requirements (§35.24 to §35.59)
- SUBPART C—General Technical Requirements (§35.60 to §35.92)
- SUBPART D—Unsealed Byproduct Material—Written Directive Not Required (§35.100 to §35.290)
- SUBPART E—Unsealed Byproduct Material—Written Directive Required (§35.300 to §35.396)
- SUBPART F—Manual Brachytherapy (§35.400 to §35.491)
- SUBPART G—Sealed Sources for Diagnosis (§35.500 to §35.590)
- SUBPART H—Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units (§35.600 to §35.690)
- SUBPART K—Other Medical Uses of Byproduct Material or Radiation From Byproduct Material (§35.1000 to §35.1000)
- SUBPART L—Records (§35.2024 to §35.2655)
- SUBPART M—Reports (§35.3045 to §35.3067)
- SUBPART N—Enforcement (§35.4001 to §35.4002)