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Webinar

NGS for GMP compliance: New guidelines, new tools

Upcoming
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Apr 14, 2026
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9:00 AM (GMT+0)
+1 other
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You will learn

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The impact of current guidelines, including ICH Q5A(R2), FDA 21 CFR Part 11 and European Pharmacopeia Chapter 2.6.41 on biologics production

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Key requirements on data integrity, audit trails, user authentication and more, for setting up GxP environments

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How QIAGEN CLC Genomics Workbench and Server support achieving GxP compliance

About this webinar

The updated ICH Q5A(R2) guidelines recommend next-generation sequencing (NGS) as the preferred approach for detecting adventitious agents. From cell line development and viral clearance studies to contamination tracing and product characterization, NGS-based tests outperform older assays in efficacy, sensitivity and reproducibility. This forms the basis for implementation by leading regulatory authorities, including the FDA, EMA, PMDA, and MFDS, signaling a global shift in biosafety testing.

Ensure easy compliance with these new directives by using a robust, computer systems validation (CSV)-friendly software platform that supports transparency and traceability throughout your biologics production pipeline.

Speakers

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