Part 212 - CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
- Subpart A - GENERAL PROVISIONS (§§ 212.1 — 212.5)
- Subpart B - PERSONNEL AND RESOURCES (§ 212.10)
- Subpart C - QUALITY ASSURANCE (§ 212.20)
- Subpart D - FACILITIES AND EQUIPMENT (§ 212.30)
- Subpart E - CONTROL OF COMPONENTS, CONTAINERS, AND CLOSURES (§ 212.40)
- Subpart F - PRODUCTION AND PROCESS CONTROLS (§ 212.50)
- Subpart G - LABORATORY CONTROLS (§§ 212.60 — 212.61)
- Subpart H - FINISHED DRUG PRODUCT CONTROLS AND ACCEPTANCE (§§ 212.70 — 212.71)
- Subpart I - PACKAGING AND LABELING (§ 212.80)
- Subpart J - DISTRIBUTION (§ 212.90)
- Subpart K - COMPLAINT HANDLING (§ 212.100)
- Subpart L - RECORDS (§ 212.110)