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MFG MANUAL - 005 Storage, Handling and Cleaning of Hoses Used in Pharmaceutical Production

MFG MANUAL - 007 Maintenance and Calibration of GMP Critical Item

MFG MANUAL - 003 Manufacturing Documentation

MFG MANUAL - 033 Use and Recovery of Solvents in API Manufacturing

MFG MANUAL - 009 Cleaning and Sterilization of Aseptic Manufacturing Equipment

MFG MANUAL - 017 Preventing Cross Contamination

MFG MANUAL - 011 Defining Worst Case Conditions for Aseptic Process Simulations

MFG MANUAL - 008 Clean Steam Systems

MFG MANUAL - 022 Returned Goods

MFG MANUAL - 014 Retreatment and Blending of API & Formulated Product

MFG MANUAL - 018 In-Process Testing, Checks and Sampling

MFG MANUAL - 016 Packaging System Integrity for Sterile Medical Devices

MFG MANUAL - 010 Container Closure Integrity for Sterile Drug Products

MFG MANUAL - 024 Receipt Handling and Storage of Starting & Packaging Materials

MFG MANUAL - 013 Validation of Lyophilization Processes

MFG MANUAL - 029 Assessment of Shipping Processes for Drug Products

MFG MANUAL - 019 Prevention and Control of Fungal Contamination in Tablets

MFG MANUAL - 026 Control of Packaging Operation

MFG MANUAL - 004 Installation, Use and Maintenance of Metal Detectors in Pharmaceutical

MFG MANUAL - 002 Management of Non-Sterile Active Pharmaceutical Ingredient Manufacturing Area

MFG MANUAL - 023 Unplanned Cleanroom Power Outage Time Limit and Recovery

MFG MANUAL - 021 Sterilization or Depyrogenation Validation for Non Product Components

MFG MANUAL - 028 Requirements for Facilities For Sterile and Non-sterile Drug Manufacture

MFG MANUAL - 034 Principles and Responsibilities for The Management of Change in Operations

MFG MANUAL - 032 Sterile & Non Sterile Vial Capping Operations

MFG MANUAL - 030 Cold Chain Management of Biopharmaceutical Materials

MFG MANUAL - 012 Gamma Radiation Sterilization

MFG MANUAL - 020 Sanitant Rotation in a Routine Sanitization Program

MFG MANUAL - 015 Lyophilizer Loading and Unloading Recommendations

MFG MANUAL - 031 Labeling and Packaging of Investigational Medicinal Products and APIs in R&D

MFG MANUAL - 006 Alternatives to Formaldehyde Fogging of Clean Rooms

MFG MANUAL - 001 Considerations for Selecting Packaging Lot Sizes During Packaging

MFG MANUAL - 027 Water Activity Fundamentals and Applications in Pharmaceutical Operations

MFG MANUAL - 025 Use of Sterilized Goggles Within the Aseptic Processing Area

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