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1.0 - Dietary Supplement 21 CFR 111 Definitions
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1.0 - Drug Definitions used in 21 CFR 211
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1.1 - Quality Management System (QMS) Overview
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1.2 - Good Manufacturing Practice GMP
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1.4 - Product Quality Review (PQR)
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1.6 - Good Distribution Practice GDP
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1.7 - Self Inspection via Internal Audits
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10.0 - Returned and Salvaged Drug Products
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10.2 - Outsourced GMP Activities
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10.3 - Laboratory Specifications
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10.4 - Laboratory OOS Investigation & Form
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10.5 - Laboratory Physical and Chemical Testing
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10.6 - Laboratory Microbiology Testing Overview
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10.7 - Laboratory Stability Testing
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10.8 - Laboratory Method Validation
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11.0 - Manufacturing Operations
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12.0 - Packaging and Labelling Operations
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13.0 - Warehouse Holding Requirements
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13.1 - Distribution and Good Distribution Practice (GDP)
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14.0 - Returned Dietary Supplements
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15.0 - Product Complaints Handling
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16.0 - GMP Records for Supplements
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2.0 - Personnel Qualifications and Training
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2.1 - Personnel and Visitor Sickness Policy
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2.1 - Production & Quality Management
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2.2 - Personnel Hygiene and Dress Code
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3.0 - Buildings and Facilities Overview
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3.0 - Facility Design and Construction
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3.1 - Yard and Grounds Maintenance
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3.2 - Buildings and Facilities - Laboratory
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3.3 - Buildings and Facilities - Holding and Distribution
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3.3 - Cleaning & Sanitizing Agents
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3.4 - Buildings and Facilities - Pest Control
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