Level
Introductory
Format
On-site, practical, including essential theory
Duration
2 days
Cost
$1,881
Overview
Biomanufacturing requires the production of both excipients and final products in liquid form. Managing solutions at industrial scale—whether in pilot or commercial operations—demands well-planned, quality-driven practices to maintain sterility throughout the process and mitigate contamination risks. This course offers a solid foundational understanding of cleanroom classifications, contamination control strategies, and sterilization methods essential for aseptic liquid handling and transfer.
Why It’s Essential
Failing to incorporate sterility assurance at the appropriate manufacturing steps can lead to costly corrective actions downstream. A preventive approach is the most effective strategy, ensuring issues are avoided before they compromise product quality or require significant remediation.
Learning Objectives
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Cleanroom classification and contamination control
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Aseptic processing and biopharmaceutical regulations
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Aseptic solution transfer, tube welding and aseptic connection types
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Internalizing sterility-assurance principles that regulators scrutinize
Who Should Attend
Biomanufacturing operators, QA/QC personnel, and production supervisors.
Participants who successfully complete a theoretical assessment will receive a certificate of completion.

