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All Products
VAL MANUAL- 013 USD 12
VAL MANUAL- 001 USD 8
VAL MANUAL- 010 USD 8
VAL MANUAL- 044 USD 8
VAL MANUAL- 011 USD 8
VAL MANUAL- 036 USD 8
VAL MANUAL- 006 USD 8
VAL MANUAL- 025 USD 8
VAL MANUAL- 054 USD 8
VAL MANUAL- 016 USD 10
VAL MANUAL- 008 USD 8
VAL MANUAL- 004 USD 6
VAL MANUAL- 020 USD 8
VAL MANUAL- 019 USD 8
VAL MANUAL- 022 USD 8
VAL MANUAL- 005 USD 7
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VAL MANUAL- 041 USD 7
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VAL MANUAL- 048 USD 8
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VAL MANUAL- 021 USD 12
VAL MANUAL- 028 USD 10
VAL MANUAL- 009 USD 8
VAL MANUAL- 002 USD 6
VAL MANUAL- 038 USD 8
VAL MANUAL- 049 USD 6
VAL MANUAL- 018 USD 8
VAL MANUAL- 043 USD 8
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VAL MANUAL- 031 USD 7
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VAL MANUAL- 027 USD 8
VAL MANUAL- 053 USD 10
VAL MANUAL- 007 USD 4
VAL MANUAL- 056 USD 8
VAL MANUAL- 037 USD 4
VAL MANUAL- 033 USD 8
VAL MANUAL- 014 USD 6
VAL MANUAL- 047 USD 5
VAL MANUAL- 042 USD 7
VAL MANUAL- 015 USD 8
VAL MANUAL- 055 USD 8
VAL MANUAL- 057 USD 8
VAL MANUAL- 060 USD 8
VAL MANUAL- 035 USD 7
VAL MANUAL- 026 USD 5
VAL MANUAL- 032 USD 8
VAL MANUAL- 051 USD 5
VAL MANUAL- 052 USD 8
VAL MANUAL- 012 USD 8
VAL MANUAL- 046 USD 8
VAL MANUAL- 029 USD 8
VAL MANUAL- 003 USD 8
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VAL MANUAL- 061 USD 10
VAL MANUAL- 013 Cleaning and Cleaning Validation of API Plant and Equipment
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VAL MANUAL- 001 The Preparation of Validation Master Plan
USD 6.00
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VAL MANUAL- 010 Batch Homogeneity Demonstration of Active Pharmaceutical Ingredient Preparation
USD 6.00
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VAL MANUAL- 044 Documenting IQ, OQ, PQ Protocol Test Results for Equipment, Facility and Computer
USD 6.00
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VAL MANUAL- 011 Documentation Models for Continuous Quality Verification
USD 6.00
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VAL MANUAL- 036 Information Technology Infrastructure Qualification
USD 6.00
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VAL MANUAL- 006 Evaluation of Changes for Potential Impact on Process Validation
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VAL MANUAL- 025 Periodic Review Process of Validated Equipment and Computer Systems in Pharmaceutical Industry
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VAL MANUAL- 054 Procedure for Identification and Sampling of Swab and Visual Inspection Locations for Medicinal Products and API Equipment
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VAL MANUAL- 016 Sterilization Process Validation
USD 7.00
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VAL MANUAL- 008 In-Process and Bulk Drug Product Holding Times
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VAL MANUAL- 004 Evaluating Non-Cleaned Equipment Hold Times for Cleaning Validation Medicinal Products
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VAL MANUAL- 020 Process Validation Sampling Practices for Non-Sterile Liquid and Semi Solid Drug Products
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VAL MANUAL- 019 Cleaning and Cleaning Validation For Formulated Products
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VAL MANUAL- 022 Process Validation Sampling for Non-Sterile Solid Dose Drug Products
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VAL MANUAL- 005 Process Validation of Bulk Drug (API and Intermediate)
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VAL MANUAL- 023 Performance Qualification versus Process Validation
USD 4.00
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VAL MANUAL- 050 Systems Validation
USD 6.00
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VAL MANUAL- 041 Clean Pure Steam System Commissioning and Qualification Approaches & Sampling Plans
USD 7.00
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VAL MANUAL- 017 Matrices and Bracketing of Medicinal Products in Process Validation
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VAL MANUAL- 048 Purified Water and Water for Injection System Commissioning and Qualification Sampling Plans
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VAL MANUAL- 045 Access by Regulatory Authorities and Auditors to Electronic Records
USD 6.00
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VAL MANUAL- 058 Documentation and Records for Cleaning Activities and Evaluation
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VAL MANUAL- 059 Identifying Critical Process Parameters for Manufacturing of Medicinal Products
USD 7.00
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VAL MANUAL- 021 Principle and Precedures of Analytical Test Method Validation for GMP Regulated Industry
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VAL MANUAL- 028 The validation of facilities and system
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VAL MANUAL- 009 Process Validation for Formulated Products
USD 6.00
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VAL MANUAL- 002 Clean Equipment Hold Times Establishment and Practices
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VAL MANUAL- 038 Validation Considerations for Transportation of Biopharmaceutical Materials
USD 6.00
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VAL MANUAL- 049 Quality Considerations for Direct Impact Compressed Air and Nitrogen Systems
USD 6.00
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VAL MANUAL- 018 Potential Critical Packaging Process Parameters and Validation Practices
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VAL MANUAL- 043 Cycle Validation for Freeze Drying
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VAL MANUAL- 024 General Outline of Analytical Procedure Validation
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VAL MANUAL- 040 Management of Change in Computerised System
USD 7.00
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VAL MANUAL- 030 Identification and Investigation of Test Deviations During Validation
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VAL MANUAL- 031 Validation Activities during Technology Transfers
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VAL MANUAL- 039 System Level Impact Assessment for Information Systems
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VAL MANUAL- 027 Potential Critical Parameters for ProcessIinvolves in Formulating Solid Oral Dosage Forms
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VAL MANUAL- 053 Calculations of Residue Limits for Medicinal Product for Equipment Cleaning During Cleaning Validation
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VAL MANUAL- 007 Swab and Visual Inspection Sampling Locations Guidance for Process Equipment
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VAL MANUAL- 056 Rinsate and Swab Sampling Procedure in Test Method Development and Validation
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VAL MANUAL- 037 How to Investigate Unknown Chromatographic Peaks during Cleaning Validation Activity
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VAL MANUAL- 033 Validation Documentation
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VAL MANUAL- 014 Guidance on Selection Criteria of Dose and Toxicity Data
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VAL MANUAL- 047 Packaging Process Documentation Transfer for Drug Products
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VAL MANUAL- 042 Component Level Impact Assessment for Information System Application
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VAL MANUAL- 015 Inspection Attributes in Packaging Validation of Non-Sterile Drug Products
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VAL MANUAL- 055 How to Group Product and Equipment and Select the Worst Case Product in Cleaning Validation
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VAL MANUAL- 057 Method of Visual Inspection and Quantitation in Cleaning Validation
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VAL MANUAL- 060 Process Validation Approaches for Formulated Medicinal Products and Medical Devices
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VAL MANUAL- 035 Non-Sterile API Manufacturing Area Environmental Control
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VAL MANUAL- 026 Critical Parameters for Process Involves in Formulating Semi-Solid Dosage Forms
USD 5.00
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VAL MANUAL- 032 Validation Considerations for Re-work and Re-process of API
USD 6.00
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VAL MANUAL- 051 Implementation of Process Analytical Technology
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VAL MANUAL- 052 Validation of Process Analytical Technology System
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VAL MANUAL- 012 Documentation to Foster Continuous Quality Verification
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VAL MANUAL- 046 Material of Construction Documentation
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VAL MANUAL- 029 Examples and Approaches of Solvent Recovery Validation
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VAL MANUAL- 003 Equivalency Comparison of Medicinal Product Validation Batch Data to Reference Batches
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VAL MANUAL- 034 Demonstration and Calculation of Equivalence Criteria of Impurities for API Process Validation
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VAL MANUAL- 062 Use of Process Analytical Technology in Process Validation
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VAL MANUAL- 061 Cleaning Validation and Verification of Equipments Used for Manufacturing Active Pharmaceutical Ingredients
USD 7.00
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