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Webinars

Upcoming Webinars

  • Is There a Gap in Your Process Validation?

    Date: November 14 2017 - 3PM London / 10AM New York

    Key learning objectives:

    Understand the factors that should be considered when validating a single-use process
    Find out how to increase performance through consideration of broader design elements
    Learn how to ensure single-use assemblies are validated for the entire supply chain

  • A Novel Approach to Single-Use Design and Implementation

    Date: October 25, 2017 - 4PM London / 11AM New York

    Key learning objectives:

    Learn how to quickly and easily implement single-use technology
    Understand how to simplify your supply chain

    Learn how to ensure compliance of your single-use devices

Missed a webinar? View on demand here

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    Protect the Process; Protect the Patient

    Discussing how elements of process protection come together to ensure the provision of critical biopharmaceuticals to those that need them.
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    Single-Use Technology, What's Next?

    What developments are needed for the further implementation of single-use technology and what is stopping us getting there?
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    Standardization in a Custom World

    Discussing opportunities for standardization that will speed up and simplify the implementation of your single-use projects.
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    Application of QbD Concepts

    Discussing points to consider when implementing QbD into your bioprocess with reference to the example of a final sterilizing grade filtration step.
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    Developing Single-Use TFF Steps

    Highlighting best practices for developing single-use TFF steps from filter selection to GMP implementation.
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    Preventing Mycoplasma Contamination

    Presenting practical strategies for implementing a risk-management based approach to preventing Mycoplasma Contaminations.
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