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#GMP Manuals and Practical Guidance

USD 8.00
#GMP Manuals and Practical Guidance#Analytical Microbiology Laboratory Manuals#LAB MANUAL - 010 USD 8
LAB MANUAL - 010 Preparation & Maintenance of Stability Protocols and Stability Master Plans
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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#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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#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- 024 USD 5
QMS MANUAL- 024 Warehousing and Distribution of Commercial Products
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#GMP Manuals and Practical Guidance#Analytical Microbiology Laboratory Manuals#LAB MANUAL - 026 USD 8
LAB MANUAL - 026 Out of Specification Results Investigation
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#GMP Manuals and Practical Guidance#Analytical Microbiology Laboratory Manuals#LAB MANUAL - 015 USD 8
LAB MANUAL - 015 Explanation of Repeat Testing and Retesting Utilized During
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 009 USD 8
QMS MANUAL- 009 Quality Agreements - PART 1
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#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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#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#Quality Management Systems Manuals#QMS MANUAL- 010 USD 8
QMS MANUAL- 010 Quality Agreements - PART 2
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#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#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 017 USD 4
MFG MANUAL - 017 Preventing Cross Contamination
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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- 008 USD 8
VAL MANUAL- 008 In-Process and Bulk Drug Product Holding Times
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#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#Quality Management Systems Manuals#QMS MANUAL- 058 USD 5
QMS MANUAL- 058 Calibration
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 055 USD 5
QMS MANUAL- 055 Preventive Maintenance
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#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 044 USD 8
VAL MANUAL- 044 Documenting IQ, OQ, PQ Protocol Test Results for Equipment, Facility and Computer
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 009 USD 4
MFG MANUAL - 009 Cleaning and Sterilization of Aseptic Manufacturing Equipment
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 013 USD 8
MFG MANUAL - 013 Validation of Lyophilization Processes
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 018 USD 4
MFG MANUAL - 018 In-Process Testing, Checks and Sampling
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 023 USD 8
MFG MANUAL - 023 Unplanned Cleanroom Power Outage Time Limit and Recovery
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 015 USD 5
MFG MANUAL - 015 Lyophilizer Loading and Unloading Recommendations
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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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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 047 USD 5
QMS MANUAL- 047 Management of Master GMP Document
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 038 USD 4
QMS MANUAL- 038 Definition and Documentation of Raw Data
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 010 USD 5
MFG MANUAL - 010 Container Closure Integrity for Sterile Drug Products
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USD 4.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 032 USD 4
MFG MANUAL - 032 Sterile & Non Sterile Vial Capping Operations
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 023 USD 4
QMS MANUAL- 023 Receipt, Approval and Use of Labels and Labeling
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USD 3.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 032 USD 3
QMS MANUAL- 032 Pest Control
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#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 003 USD 8
MFG MANUAL - 003 Manufacturing Documentation
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 048 USD 5
QMS MANUAL- 048 Artwork Creation & Control of Printed Packaging Components
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USD 6.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 019 USD 6
MFG MANUAL - 019 Prevention and Control of Fungal Contamination in Tablets
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#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 052 USD 8
QMS MANUAL- 052 Deviation Management
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USD 7.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 041 USD 7
QMS MANUAL- 041 Risk Management in the Quality and Compliance Area
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