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Introduction to FDA CFR 210 and 211
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Introduction to FDA CFR 210 and 211
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Subpart D – Equipment
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Subpart F – Production and Process Controls
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Chapter
Introduction of Part 210
The Definitions – 210.3
PART 211
Subpart A – General Provisions
Subpart B – Organization and Personnel
Subpart C – Buildings and Facilities
Subpart D – Equipment
Subpart E – Control of Components and Drug Product Containers and Closures
Subpart F – Production and Process Controls
Subpart G – Packaging and Labeling Control
Subpart H – Holding and Distribution
Subpart I – Laboratory Controls
Subpart J – Records and Reports
Subpart K – Returned and Salvaged Drug Products
9. EVALUATION QUESTIONNAIRE
10 questions
