

Aseptic behavior remains a critical element of contamination control in modern healthcare and pharmaceutical manufacturing. With increasing process complexity and regulatory expectations—particularly under EU GMP Annex 1—focus is shifting toward human factors, system design, standardization, and data-driven monitoring. This webinar addresses current directions in aseptic performance, emphasizing process reliability, risk reduction, and practical alignment with Annex 1 principles.
Our Focus:
This webinar is intended for professionals involved in aseptic operations, contamination control, and quality oversight. It is relevant for personnel working in pharmaceutical manufacturing, sterile product processing, quality assurance, quality control, engineering, and regulatory compliance. The content is also applicable to leaders responsible for system design, process reliability, and Annex 1 implementation.
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