Pharmaceutical master validation plan : the ultimate guide to FDA, GMP, and GPL compliance The Ultimate Guide to FDA, GMP, and GLP Compliance

The Master Validation Plan provides a roadmap to management for on-time start-up of facility operations, and validation of existing facilities, in compliance with GMP requirements. The lack of a comprehensive Master Validation Plan and well-documented validation procedures is the main reason that new drug, medical device, medical equipment, and related product applications are rejected by the FDA. In fact, only about 2% of the applications submitted by foreign pharmaceutical companies are approved each year. This thorough guide provides the needed solutions and guidance for both foreign and U.S. companies to achieve FDA compliance and authorization to market their products in the United States. Pharmaceutical Master Validation Plan: The Ultimate Guide to FDA, GMP, and GLP Compliance will allow you to more easily achieve satisfactory inspections, new medical product approval, minimize non-conformance, reduce rework and rejected lots, and avoid recall lots by developing and managing a Master Validation Plan. The accompanying CD allows users to input the template plan into their computers and tailor it to incorporate additional regulatory requirements specific to individual companies worldwide and print the required documents. Together, the book and CD contain everything required to develop and execute a successful Master Validation Plan based on FDA guidelines for the pharmaceutical industry, and allows the templates to be extended to diagnostic products, medical device, medical equipment, and biotech industry products.

IntroductionProject Description What is a Validation Master Plan Scope of a Validation Master Plan Definition of the Term Validation Validation Team Members Validation Team Responsibilities Concept of qualification / validationFundamentals Concept of a Validation Life Cycle Elements of Qualification/Validation Documentation Format of Qualification Programs Numbering System RevalidationResponsibilitiesFacility descriptionLine Capacities Description of buildingDry Production Facility: Building A Liquid and Semisolid Production Facility: Building B Parenterals Production Facility: Building C Equipment descriptionDry Production Facility: Building A Liquid and Semisolid Production Facility: Building B Parenterals Production Facility: Building C Over- Printing Area Quality Control Quality Assurance (In-Process) Product Development Laboratories Hvac descriptionDry Production Facility: Building A Liquid and Semisolid Production Facility: Building B Parenterals Production Facility: Building C Over-Printing Area Quality Control Quality Assurance (In-Process) Product Development Laboratories Utilities descriptionDeionized Water (DI Water) Purified Water Water for Injection (WFI) Chilled Water Pure Steam Compressed Air Nitrogen (N2) Carbon Dioxide (CO2) Electric Power Sanitary Water HVAC (Heating, Ventilation, and Air Conditioning) System Validation program overviewValidation Project Management: Organization Validation Responsibilities Design and Validability Review Validation Documents Installation Qualification Protocols Operational Qualification Protocols Change Control Initiation Cycle Development Performance Qualification Protocols Process Validation Protocols Validation Final Reports Validation Package Certificate for Use in Manufacturing Required Protocols and Procedures for Dry Production: Building A Required Protocols and Procedures for Liquid and Semisolid Production: Building B Required Protocols and Procedures for Parenterals Production: Building C Calibration program summaryPreventative maintenance program summaryKey standard operating procedures (sops)Validation of buildingCivil Work Drainage System Validation of utility systemsPlant Steam Pure Steam Water for Injection (WFI) Compressed Air Nitrogen (N2) Heating Ventilation and Air Conditioning (HVAC) Emergency Power (Standby Generator) Process description building a dry production: building aProcess Flow, Variables and Responses: Tablets Process Flow, Variables and Responses Powder for Suspension Process Flow, Variables and Responses: Capsules Process description liquid and semisolid production: building bProcess Flow, Variables, and Responses: Syrup, Suspension, and Drop Products Process Flow, Variables and Responses: Cream Ointment, and Suppository Products Process description for parenterals production facility: building cProcess Flow, Variables, and Responses: Aseptic Fill Products Process Flow, Variables, and Responses: Ready-to-Use Disposable Syringes Process Flow, Variables, and Responses: Terminal Sterilization Products Process Flow, Variables and Responses: Lyophilized Products Qualification of process equipmentCommuting Mill Dryer V-Shell Blender Tablet Compression Capsulation Powder Filing Capsule Polisher Tablet Coating Syrup Manufacturing Vessel Suspension Manufacturing Vessel Drops Manufacturing Vessel Mixer Filter Press Cream/Ointment/Suppository Manufacturing Vessel Syrup, Suspension, and Drop Filling Machine Cream and Ointment Filling Machine Suppository Filling Machine Labeling Machine Capping Machine Cartonator Shrink-Wrapping Machine Over-Printing Machine Autoclave (Steam Sterilizer) Hot Air Tunnel (Dry Heat Sterilizer) Vials / Ampoules Washing Machine Vials / Ampoules / Syringes Filling Machine Freeze Dyer (Lyophilizer) Laminar Flow Unit Pass Through Validation of support processWashing of Components Sterilization of Components Depyrogenation of Components Aseptic Filling Validation (Media Fill Studies) Cross-Contamination Control Computerized Pharmaceutical System Quality assurance / control laboratory validationLaboratory Equipment Qualification Computer Related Systems in QA/QC Laboratory Cgmp procedures and programsEngineering Change Control Calibration Preventive Maintenance Program Standard Operating Procedure (SOPs) Facility Cleaning and Sanitization Environmental Monitoring Program Hepa filter integrity testingFilter Integrity Testing Label Control Program cGMP Training Equipment Log Book, Status Tags, and Room Clearance Checklists Validation Files Validation scheduleDrawings for abc pharmaceutical plantIndex

Healthcare management quality assurance managers, operations managers, executives, and quality engineers; validation designers, internal auditors, and external auditors; industrial engineers and manufacturing engineers; mechanical engineers, computer engineers, utilities engineers; chemical engineers