Part 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
- Subpart A - GENERAL PROVISIONS (§§ 211.1 — 211.3)
- Subpart B - ORGANIZATION AND PERSONNEL (§§ 211.22 — 211.34)
- Subpart C - BUILDINGS AND FACILITIES (§§ 211.42 — 211.58)
- Subpart D - EQUIPMENT (§§ 211.63 — 211.72)
- Subpart E - CONTROL OF COMPONENTS AND DRUG PRODUCT CONTAINERS AND CLOSURES (§§ 211.80 — 211.94)
- Subpart F - PRODUCTION AND PROCESS CONTROLS (§§ 211.100 — 211.115)
- Subpart G - PACKAGING AND LABELING CONTROL (§§ 211.122 — 211.137)
- Subpart H - HOLDING AND DISTRIBUTION (§§ 211.142 — 211.150)
- Subpart I - LABORATORY CONTROLS (§§ 211.160 — 211.176)
- Subpart J - RECORDS AND REPORTS (§§ 211.180 — 211.198)
- Subpart K - RETURNED AND SALVAGED DRUG PRODUCTS (§§ 211.204 — 211.208)