StacksVerified U.S. regulatory reference

Part 35 — Medical Use of Byproduct Material

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 K — Other Medical Uses of Byproduct Material or Radiation From Byproduct Material

Subpart L — Records

Subpart M — Reports

Subpart N — Enforcement