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#GMP Manuals and Practical Guidance

USD 8.00
#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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USD 5.00
#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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USD 8.00
#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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USD 8.00
#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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USD 8.00
#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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USD 12.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 013 USD 12
VAL MANUAL- 013 Cleaning and Cleaning Validation of API Plant and Equipment
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 010 USD 8
VAL MANUAL- 010 Batch Homogeneity Demonstration of Active Pharmaceutical Ingredient Preparation
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 011 USD 8
VAL MANUAL- 011 Documentation Models for Continuous Quality Verification
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USD 8.00
#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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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 008 USD 8
VAL MANUAL- 008 In-Process and Bulk Drug Product Holding Times
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 020 USD 8
VAL MANUAL- 020 Process Validation Sampling Practices for Non-Sterile Liquid and Semi Solid Drug Products
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USD 8.00
#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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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 019 USD 8
VAL MANUAL- 019 Cleaning and Cleaning Validation For Formulated Products
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 017 USD 8
VAL MANUAL- 017 Matrices and Bracketing of Medicinal Products in Process Validation
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USD 4.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 023 USD 4
VAL MANUAL- 023 Performance Qualification versus Process Validation
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USD 8.00
#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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USD 12.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 021 USD 12
VAL MANUAL- 021 Principle and Precedures of Analytical Test Method Validation for GMP Regulated Industry
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USD 4.00
#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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USD 10.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 028 USD 10
VAL MANUAL- 028 The validation of facilities and system
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 009 USD 8
VAL MANUAL- 009 Process Validation for Formulated Products
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USD 8.00
#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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USD 6.00
#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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USD 8.00
#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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USD 5.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 026 USD 5
VAL MANUAL- 026 Critical Parameters for Process Involves in Formulating Semi-Solid Dosage Forms
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USD 8.00
#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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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 067 USD 8
QMS MANUAL- 067 Electronic Records and Electronic Signatures
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USD 8.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 001 USD 8
VAL MANUAL- 001 The Preparation of Validation Master Plan
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USD 6.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 056 USD 6
QMS MANUAL- 056 Batch Confirmation Certification & Release by a Qualified Person within the EU
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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 060 USD 8
QMS MANUAL- 060 Guideline for Development and Contents of Specifications
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USD 5.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 057 USD 5
QMS MANUAL- 057 Cross Contamination Risk Evaluation Process for Commercial Compounds
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USD 7.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 062 USD 7
QMS MANUAL- 062 Certificate of Analysis & Certificate of Manufacture
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USD 4.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 061 USD 4
QMS MANUAL- 061 R&D QA Audits for Suppliers and Vendors
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USD 6.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 004 USD 6
VAL MANUAL- 004 Evaluating Non-Cleaned Equipment Hold Times for Cleaning Validation Medicinal Products
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USD 5.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 055 USD 5
QMS MANUAL- 055 Preventive Maintenance
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USD 6.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 059 USD 6
QMS MANUAL- 059 Evaluation Process Supporting Elimination of Defined Shipment Temperature Range
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USD 7.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 005 USD 7
VAL MANUAL- 005 Process Validation of Bulk Drug (API and Intermediate)
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