Code of Federal Regulations · Part

Part 35 — Medical Use Of Byproduct Material

10 C.F.R. pt. 35

• Subpart A General Information
• Subpart B General Administrative Requirements
• Subpart C General Technical Requirements
• Subpart D Unsealed Byproduct Material—written Directive Not Required
• Subpart E Unsealed Byproduct Material—written Directive Required
• Subpart F Manual Brachytherapy
• Subpart G Sealed Sources For Diagnosis
• Subpart H Photon Emitting Remote Afterloader Units, Teletherapy Units, And Gamma Stereotactic Radiosurgery Units
• Subpart I-J Subparts I-j [reserved]
• Subpart K Other Medical Uses Of Byproduct Material Or Radiation From Byproduct Material
• Subpart L Records
• Subpart M Reports
• Subpart N Enforcement