Federal (United States) · Regulations
Part 35 — MEDICAL USE OF BYPRODUCT MATERIAL
111 sections
12 groups
- Subpart A — General Information14 sections
- Subpart B — General Administrative Requirements11 sections
- Subpart C — General Technical Requirements10 sections
- Subpart D — Unsealed Byproduct Material—Written Directive Not Required5 sections
- Subpart E — Unsealed Byproduct Material—Written Directive Required7 sections
- Subpart F — Manual Brachytherapy10 sections
- Subpart G — Sealed Sources for Diagnosis2 sections
- Subpart H — Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units17 sections
- Subpart K — Other Medical Uses of Byproduct Material or Radiation From Byproduct Material1 section
- Subpart L — Records28 sections
- Subpart M — Reports4 sections
- Subpart N — Enforcement2 sections