21 CFR Part 211 Subpart A General Provisions 21 CFR Part 211 Subpart B: Organization and Personnel 21 CFR Part 211 Subpart C: Building and Facilities 21 CFR Part 211 – Subpart D: Equipment 21 CFR Part 211 Subpart E: Control of Components, Drug Product Containers and Closures 21 CFR Part 211 Subpart F: Production and Process Controls 21 CFR Part 211 Subpart G: Packaging and Labeling Control 21 CFR Part 211 Subpart H: Holding & Distribution Controls 21 CFR Part 211 Subpart I: Laboratory Controls 21 CFR Part 211 Subpart J: Records and Reports 21 CFR Part 211 Subpart K: Returned and Salvaged Drug Products 21 CFR § 211.63 Equipment design, size, and location 21 CFR § 211.65 Equipment construction 21 CFR § 211.67 Equipment cleaning and maintenance 21 CFR § 211.68 Automatic, mechanical, and electronic equipment. 21 CFR § 211.70 Filters. 21 CFR § 211.22 Responsibilities of Quality Control Unit 21 CFR § 211.25 Personnel Qualifications. 21 CFR § 211.34 Consultants. 21 CFR § 211.42 Design and construction features. 21 CFR § 211.46 Ventilation, Air filtration, Air heating and Cooling. 21 CFR § 211.48 Plumbing. 21 CFR § 211.56 Sanitation. § 211.44 Lighting. § 211.50 Sewage and refuse. § 211.52 Washing and toilet facilities. § 211.58 Maintenance. 21 CFR § 211.80 Control of Components and Drug Product Containers and Closures 21 CFR § 211.82 Receipt and storage of untested components, drug product containers, and closures. 21 CFR § 211.84 Testing and approval or rejection of components, drug product containers & closures 21 CFR § 211 86 87 89, Approved, Retesting and Rejected 21 CFR § 211.100 Production and Process Controls Written procedures; deviations. 21 CFR § 211.101 Production and Process Controls Charge-in of components.