Training Event Registration Forms

  • Bethesda, MD, USA
    September 2018

    GAMP® Data Integrity 21 CFR Part 11
    10 - 12 Sept

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    Risk-Based Verification of Facilities, Systems and Equipment Workshop
    13 - 14 Sept

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    Cleaning Validation Principles
    17 - 18 Sept

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    Practical Implementation of Process Validation Lifecycle Approach
    19 - 21 Sept

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    GAMP® 5, Annex 11/Part 11 Basic Principles
    24 - 26 Sept

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    December 2018

    GAMP® 5, Annex 11/Part 11 Basic Principles
    05 - 07 Dec

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    Quality Management Systems
    10 - 11 Dec

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  • Boston, MA, USA
    October 2018

    Clean in Place Fundamentals
    15 - 16 Oct

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    OSD: Operations, Quality, Equipment and Technology
    15 - 16 Oct

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    Pharmaceutical Water Generation
    15 - 16 Oct

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    GAMP® 5, Annex 11/Part 11 Basic Principles
    15 - 17 Oct

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    GAMP® 5 GxP Process Control Systems
    17 - 18 Oct

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    Storage, Delivery and Qualification of Pharmaceutical Waters
    17 - 18 Oct

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  • Huntington Beach, CA USA
    December 2018

    Applying Biopharmaceutical Manufacturing Facilities Baseline® Guide Principles
    13–14 Dec

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    An Overview of Biopharmaceutical Manufacturing Processes
    13– 14 Dec

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    Risk-Based Verification of Facilities, Systems and Equipment Workshop
    13– 14 Dec

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    Q7A: Implementing Good Manufacturing Practices
    13–14 Dec

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  • Lyon, France
    September 2018

    Applying Biopharmaceutical Manufacturing Facilities Baseline® Guide Principles
    18–19 Sept

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    Process Validation in Biotechnology Manufacturing
    18–19 Sept

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    Science & Risk-based Commissioning & Qualification - Applying the ISPE Good Practice Guide: Applied Risk Management for Commissioning & Qualification
    18 - 19 Sept

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    Overview of Biopharmaceutical Manufacturing Processes
    18–19 Sept

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  • New Brunswick, NJ, USA
    October 2018

    GMP Sterile Pharmaceutical Manufacturing Facility
    1 - 2 Oct

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    GAMP® 5, Annex 11/Part 11 Basic Principles
    1 - 3 Oct

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    HVAC cGMP
    1 - 3 Oct

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    Practical Implementation of Process Validation Lifecycle Approach
    1 - 3 Oct

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    Applied Risk Management for Commissioning and Qualification
    3 - 4 Oct

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    Practical Application of Technology Transfer
    3 - 4 Oct

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  • Philadelphia, PA, USA
    November 2018

    Cleaning Validation Principles
    8 – 9 Nov

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    Facility Project Management in the Regulated Pharmaceutical Environment
    8 – 9 Nov

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    Quality Management Systems: Agile Approach for Product Realization & Lifecycle Management
    8 – 9 Nov

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    Risk-Based Verification of Facilities, Systems and Equipment Workshop
    8 – 9 Nov

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  • Vienna, Austria
    November 2018

    Process Validation in Biotechnology Manufacturing
    26 - 27 Nov

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    A Risk-Based Approach to GxP Process Control Systems: Applying the GAMP® Good Practice Guide: A Risk-Based Approach to GxP Process Control Systems (2nd Edition)
    26 - 27 Nov

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    Quality Management Systems: Agile Approach for Product Realization & Lifecycle Management
    26 - 27 Nov

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    Managing the Risk of Cross Contamination: Applying the Risk-MaPP Baseline® Guide
    26 - 27 Nov

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    Sterile Product Manufacturing Facilities: Applying the ISPE Baseline® Guide and FDA Guidance Principles to Design and Operation
    26 - 27 Nov

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