Part 35 - MEDICAL USE OF BYPRODUCT MATERIAL
- Subpart A - GENERAL INFORMATION (§§ 35.1 — 35.19)
- Subpart B - GENERAL ADMINISTRATIVE REQUIREMENTS (§§ 35.24 — 35.59)
- Subpart C - GENERAL TECHNICAL REQUIREMENTS (§§ 35.60 — 35.92)
- Subpart D - UNSEALED BYPRODUCT MATERIAL-WRITTEN DIRECTIVE NOT REQUIRED (§§ 35.100 — 35.290)
- Subpart E - UNSEALED BYPRODUCT MATERIAL-WRITTEN DIRECTIVE REQUIRED (§§ 35.300 — 35.396)
- Subpart F - MANUAL BRACHYTHERAPY (§§ 35.400 — 35.491)
- Subpart G - SEALED SOURCES FOR DIAGNOSIS (§§ 35.500 — 35.590)
- Subpart H - PHOTON EMITTING REMOTE AFTERLOADER UNITS, TELETHERAPY UNITS, AND GAMMA STEREOTACTIC RADIOSURGERY UNITS (§§ 35.600 — 35.690)
- Subpart K - OTHER MEDICAL USES OF BYPRODUCT MATERIAL OR RADIATION FROM BYPRODUCT MATERIAL (§ 35.1000)
- Subpart L - RECORDS (§§ 35.2024 — 35.2655)
- Subpart M - REPORTS (§§ 35.3045 — 35.3204)
- Subpart N - ENFORCEMENT (§§ 35.4001 — 35.4002)