Are your NGS workflows ready for GMP?

As regulatory expectations for cell and gene therapies evolve, robust bioinformatics workflows are critical for ensuring product quality, safety, and compliance.

Join this webinar to explore how organizations are optimizing their sequence analysis workflows to support GMP requirements, improve data integrity, and streamline decision-making throughout development and manufacturing. Topics include validated bioinformatics pipelines, variant analysis, quality analytics, and strategies for building confidence in NGS-driven processes.

This is a valuable opportunity for professionals in Regulatory Affairs, Quality, CMC, Manufacturing, or Bioinformatics to learn how modern NGS analysis approaches can support regulatory readiness.

Learn more and register: https://bpi.bioprocessintl.com/be-gmp-ready-how-to-optimize-your-sequence-analysis-workflow?utm_source=qiagen&utm_medium=email&utm_campaign=sponsor