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LAB MANUAL - 026 USD 8
LAB MANUAL - 001 USD 8
LAB MANUAL - 024 USD 10
LAB MANUAL - 002 USD 8
LAB MANUAL - 008 USD 5
LAB MANUAL - 015 USD 8
LAB MANUAL - 010 USD 8
LAB MANUAL - 023 USD 6
LAB MANUAL - 017 USD 8
LAB MANUAL - 007 USD 8
LAB MANUAL - 027 USD 5
LAB MANUAL - 013 USD 6
LAB MANUAL - 018 USD 8
LAB MANUAL - 022 USD 10
LAB MANUAL - 005 USD 5
LAB MANUAL - 014 USD 4
LAB MANUAL - 016 USD 8
LAB MANUAL - 012 USD 8
LAB MANUAL - 019 USD 8
LAB MANUAL - 004 USD 8
LAB MANUAL - 009 USD 4
LAB MANUAL - 011 USD 5
LAB MANUAL - 003 USD 8
LAB MANUAL - 006 USD 6
LAB MANUAL - 025 USD 6
LAB MANUAL - 021 USD 5
LAB MANUAL - 020 USD 8
LAB MANUAL - 028 USD 5
LAB MANUAL - 026 Out of Specification Results Investigation
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LAB MANUAL - 001 Environmental Monitoring
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LAB MANUAL - 024 Trending of Stability Data
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LAB MANUAL - 002 Analytical Laboratory Management
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LAB MANUAL - 008 Transfer of Analytical Methods
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LAB MANUAL - 015 Explanation of Repeat Testing and Retesting Utilized During
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LAB MANUAL - 010 Preparation & Maintenance of Stability Protocols and Stability Master Plans
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LAB MANUAL - 023 Overview of Trending of Environmental Monitoring
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LAB MANUAL - 017 Reference & Retention Samples
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LAB MANUAL - 007 Guideline for Stability Testing for R&D
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LAB MANUAL - 027 Analytical Procedures and Validation
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LAB MANUAL - 013 Commercial Stability Studies at Contractors
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LAB MANUAL - 018 Laboratory Equipment Qualification - PART 1
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LAB MANUAL - 022 Commercial Stability Testing For Formulated Products
USD 7.00
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LAB MANUAL - 005 Sterility Testing
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LAB MANUAL - 014 R&D GLP QA Record Retention Procedure
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LAB MANUAL - 016 Microbiological Testing for Non Sterile Drug Product
USD 6.00
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LAB MANUAL - 012 Commercial Stability Testing of API (Pure Bulk Drug)
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LAB MANUAL - 019 Laboratory Equipment Qualification - PART 2
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LAB MANUAL - 004 Microbiology Laboratory Management
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LAB MANUAL - 009 Storage and Expiry Dating of Analytical Reagents
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LAB MANUAL - 011 Controlling the Microbiological Quality of Solid Oral Dosage Forms
USD 5.00
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LAB MANUAL - 003 Water Quality Standard
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LAB MANUAL - 006 Endotoxin Testing
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LAB MANUAL - 025 Stability Considerations for Planned or Unplanned API Process Changes
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LAB MANUAL - 021 Microbiological Testing in Cleaning Validation for APIs and Drug Products
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LAB MANUAL - 020 Manufacture and Microbiological Testing of Sterile API & Drug Product Within R&D
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LAB MANUAL - 028 Microbial Attributes of Non Sterile Solid Materials Testing
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