High cell density culture is the new standard for the biopharmaceutical manufacturing process, but these feed streams can introduce major clarification challenges, such as high cell-based impurities, which foul traditional depth filters and reduce the capacities of the further purification process. pDADMAC is a promising solution, yet its use in GMP biomanufacturing requires clarification.
This webinar addresses an overview of key aspects of Quality by Design (QbD), Design of Experiments (DoE), risk assessments based on ICH-Q3A, and clearance test of pDADMAC use for GMP biomanufacturing. Finally, this webinar will help set you up to use pDADMAC in your GMP biomanufacturing process.
In this webinar, you will learn about:
<ul>
<li>Design of Experiments for pDADMAC use in GMP biomanufacturing</li>
<li>Risk assessment strategies for pDADMAC use in GMP biomanufacturing</li>
<li>Clearance testing of residual pDADMAC for GMP manufacturing</li>
</ul>

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<h2 class="webinar-subtitle">WEBINAR</h2>

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Webinar addresses pDADMAC use in GMP biomanufacturing, covering DoE, risk assessments, and clearance tests for high cell density cultures.

pDADMAC Flocculation Best Practices

WEBINAR