Part 213 - [Effective 12/18/2025] [Effective 12/18/2025] CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES
- Subpart A - [Effective 12/18/2025] GENERAL PROVISIONS (§§ 213.1 — 213.3)
- Subpart B - [Effective 12/18/2025] ORGANIZATION AND PERSONNEL (§§ 213.22 — 213.34)
- Subpart C - [Effective 12/18/2025] BUILDINGS AND FACILITIES (§ 213.42)
- Subpart D - [Effective 12/18/2025] EQUIPMENT (§§ 213.63 — 213.68)
- Subpart E - [Effective 12/18/2025] CONTROL OF INCOMING DESIGNATED MEDICAL GAS, COMPONENTS, AND MEDICAL GAS CONTAINERS AND CLOSURES (§§ 213.80 — 213.94)
- Subpart F - [Effective 12/18/2025] PRODUCTION AND PROCESS CONTROLS (§§ 213.100 — 213.110)
- Subpart G - [Effective 12/18/2025] PACKAGING AND LABELING CONTROL (§§ 213.122 — 213.130)
- Subpart H - [Effective 12/18/2025] HOLDING AND DISTRIBUTION (§ 213.150)
- Subpart I - [Effective 12/18/2025] LABORATORY CONTROLS (§§ 213.160 — 213.166)
- Subpart J - [Effective 12/18/2025] RECORDS (§§ 213.180 — 213.198)
- Subpart K - [Effective 12/18/2025] RETURNED AND SALVAGED MEDICAL GASES (§§ 213.204 — 213.208)