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#GMP Manuals and Practical Guidance

USD 8.00
#GMP Manuals and Practical Guidance#Analytical Microbiology Laboratory Manuals#LAB MANUAL - 020 USD 8
LAB MANUAL - 020 Manufacture and Microbiological Testing of Sterile API & Drug Product Within R&D
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USD 6.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 031 USD 6
MFG MANUAL - 031 Labeling and Packaging of Investigational Medicinal Products and APIs in R&D
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USD 10.00
#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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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 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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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 065 USD 8
QMS MANUAL- 065 Determination of Storage Periods for API Excipients Intermediates and Raw Materials
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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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#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- 060 USD 8
VAL MANUAL- 060 Process Validation Approaches for Formulated Medicinal Products and Medical Devices
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USD 8.00
#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- 033 USD 8
VAL MANUAL- 033 Validation Documentation
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 038 USD 8
VAL MANUAL- 038 Validation Considerations for Transportation of Biopharmaceutical Materials
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#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 5.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 058 USD 5
QMS MANUAL- 058 Calibration
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 007 USD 8
MFG MANUAL - 007 Maintenance and Calibration of GMP Critical Item
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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 013 USD 8
QMS MANUAL- 013 Training system for Aseptic and Preparation forAseptic Operators and Support Staff
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USD 4.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 011 USD 4
MFG MANUAL - 011 Defining Worst Case Conditions for Aseptic Process Simulations
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USD 5.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 018 USD 5
QMS MANUAL- 018 Quality and Compliance Auditing
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USD 3.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 029 USD 3
QMS MANUAL- 029 Compliance Improvements Plans
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USD 6.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 030 USD 6
QMS MANUAL- 030 Archiving, Disposal and Record Management
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 051 USD 8
QMS MANUAL- 051 Quality Risk Management Application to Identify Deviations vs. Events
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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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#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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#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- 019 USD 8
VAL MANUAL- 019 Cleaning and Cleaning Validation For Formulated Products
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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 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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#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 4.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 007 USD 4
VAL MANUAL- 007 Swab and Visual Inspection Sampling Locations Guidance for Process Equipment
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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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#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 5.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 029 USD 5
MFG MANUAL - 029 Assessment of Shipping Processes for Drug Products
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USD 8.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 028 USD 8
MFG MANUAL - 028 Requirements for Facilities For Sterile and Non-sterile Drug Manufacture
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USD 8.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 030 USD 8
MFG MANUAL - 030 Cold Chain Management of Biopharmaceutical Materials
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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 052 USD 8
QMS MANUAL- 052 Deviation Management
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