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#GMP Manuals and Practical Guidance

USD 10.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 016 USD 10
VAL MANUAL- 016 Sterilization Process Validation
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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 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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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 006 USD 8
QMS MANUAL- 006 Statistical Rationale for Raw Material Sampling
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USD 4.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 064 USD 4
QMS MANUAL- 064 Manufacture Packing and Shipping of Materials Ahead of Full QA Clearance
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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#Quality Management Systems Manuals#QMS MANUAL- 011 USD 8
QMS MANUAL- 011 Procedure for Quality Management of Contractors
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USD 10.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 059 USD 10
VAL MANUAL- 059 Identifying Critical Process Parameters for Manufacturing of Medicinal Products
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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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USD 4.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 035 USD 4
QMS MANUAL- 035 Raw Materials and Packaging Materials Receipt
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USD 5.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 024 USD 5
MFG MANUAL - 024 Receipt Handling and Storage of Starting & Packaging Materials
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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 004 USD 8
QMS MANUAL- 004 Application of Quality Risk Management to Periodic Review of SOPs
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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 3.00
#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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USD 8.00
#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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USD 8.00
#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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USD 7.00
#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 5.00
#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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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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USD 8.00
#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 6.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 034 USD 6
QMS MANUAL- 034 Conducting Investigations in a GMP Site
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USD 8.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 008 USD 8
QMS MANUAL- 008 Quality Risk Management Application Critical Instrument Calibration
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USD 10.00
#GMP Manuals and Practical Guidance#Analytical Microbiology Laboratory Manuals#LAB MANUAL - 024 USD 10
LAB MANUAL - 024 Trending of Stability Data
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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 6.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 021 USD 6
MFG MANUAL - 021 Sterilization or Depyrogenation Validation for Non Product Components
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USD 4.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 033 USD 4
MFG MANUAL - 033 Use and Recovery of Solvents in API Manufacturing
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USD 6.00
#GMP Manuals and Practical Guidance#Process, Cleaning, Method Computer Validation#VAL MANUAL- 002 USD 6
VAL MANUAL- 002 Clean Equipment Hold Times Establishment and Practices
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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 5.00
#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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USD 4.00
#GMP Manuals and Practical Guidance#Sterile Non Sterile Manufacturing Operation Manual#MFG MANUAL - 022 USD 4
MFG MANUAL - 022 Returned Goods
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USD 4.00
#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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USD 4.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 014 USD 4
QMS MANUAL- 014 Auditor Training
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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 5.00
#GMP Manuals and Practical Guidance#Quality Management Systems Manuals#QMS MANUAL- 002 USD 5
QMS MANUAL- 002 Product Quality Complaint Handling
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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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