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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 049 USD 5
QMS MANUAL- 049 Release of API Bulk Formulated Products & Part Finished Packs
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USD 7.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 061 USD 10
VAL MANUAL- 061 Cleaning Validation and Verification of Equipments Used for Manufacturing Active Pharmaceutical Ingredients
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 026 USD 4
QMS MANUAL- 026 Material Supplier Approval
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 031 USD 5
QMS MANUAL- 031 Control of Manufacturing and Packaging Defects Non Sterile
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 028 USD 3
QMS MANUAL- 028 Facility Based R&D QA Audit
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 020 USD 4
QMS MANUAL- 020 Material Status Indication
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 025 USD 6
QMS MANUAL- 025 Weighing and Measuring Practices In Manufacturing Operations
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 054 USD 8
VAL MANUAL- 054 Procedure for Identification and Sampling of Swab and Visual Inspection Locations for Medicinal Products and API Equipment
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 007 USD 8
QMS MANUAL- 007 Certificate of Materials Supplied to Receiving Site
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 056 USD 8
VAL MANUAL- 056 Rinsate and Swab Sampling Procedure in Test Method Development and Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 055 USD 8
VAL MANUAL- 055 How to Group Product and Equipment and Select the Worst Case Product in Cleaning Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 057 USD 8
VAL MANUAL- 057 Method of Visual Inspection and Quantitation in Cleaning Validation
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 003 USD 8
QMS MANUAL- 003 Evaluation of Contaminant Options for Packing of Solid Dosage Forms
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 050 USD 6
VAL MANUAL- 050 Systems Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 041 USD 7
VAL MANUAL- 041 Clean Pure Steam System Commissioning and Qualification Approaches & Sampling Plans
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 048 USD 8
VAL MANUAL- 048 Purified Water and Water for Injection System Commissioning and Qualification Sampling Plans
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 043 USD 8
VAL MANUAL- 043 Cycle Validation for Freeze Drying
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USD 7.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 040 USD 8
VAL MANUAL- 040 Management of Change in Computerised System
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 031 USD 7
VAL MANUAL- 031 Validation Activities during Technology Transfers
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USD 4.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 037 USD 4
VAL MANUAL- 037 How to Investigate Unknown Chromatographic Peaks during Cleaning Validation Activity
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 047 USD 5
VAL MANUAL- 047 Packaging Process Documentation Transfer for Drug Products
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 042 USD 7
VAL MANUAL- 042 Component Level Impact Assessment for Information System Application
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 035 USD 7
VAL MANUAL- 035 Non-Sterile API Manufacturing Area Environmental Control
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 032 USD 8
VAL MANUAL- 032 Validation Considerations for Re-work and Re-process of API
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 051 USD 5
VAL MANUAL- 051 Implementation of Process Analytical Technology
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 052 USD 8
VAL MANUAL- 052 Validation of Process Analytical Technology System
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 029 USD 8
VAL MANUAL- 029 Examples and Approaches of Solvent Recovery Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 034 USD 8
VAL MANUAL- 034 Demonstration and Calculation of Equivalence Criteria of Impurities for API Process Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 025 USD 8
VAL MANUAL- 025 Periodic Review Process of Validated Equipment and Computer Systems in Pharmaceutical Industry
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 022 USD 8
VAL MANUAL- 022 Process Validation Sampling for Non-Sterile Solid Dose Drug Products
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 018 USD 8
VAL MANUAL- 018 Potential Critical Packaging Process Parameters and Validation Practices
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 024 USD 4
VAL MANUAL- 024 General Outline of Analytical Procedure Validation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 027 USD 8
VAL MANUAL- 027 Potential Critical Parameters for ProcessIinvolves in Formulating Solid Oral Dosage Forms
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 014 USD 6
VAL MANUAL- 014 Guidance on Selection Criteria of Dose and Toxicity Data
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 015 USD 8
VAL MANUAL- 015 Inspection Attributes in Packaging Validation of Non-Sterile Drug Products
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 012 USD 8
VAL MANUAL- 012 Documentation to Foster Continuous Quality Verification
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