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| Webinar: How to Plan for Trouble-Free Filter Validation | Join Cytiva as they discuss regulatory expectations for process-specific filter validation in drug products requiring sterile filtration. Learn best practices for conducting process-specific filter studies, essential for marketing authorization applications such as NDA and MMA. Participants will learn about timing for validation, laboratory requirements, and strategies for successful implementation across various drug types, including monoclonal antibodies and advanced therapy medicinal products. Click here to learn more. |
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FOCUS ON DOWNSTREAM MANUFACTURING |
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By Ioanna Deni, BioPlan Associates, Inc. | BioPlan's 21st annual survey finds that downstream processing capacity constraints are at their lowest reported in years. |
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| mRNA Product IVT Process Insights | Article | Cytiva | In vitro transcription (IVT) allows a researcher to tailor synthesis and introduce modifications to produce a transcript. Learn about IVT along with process challenges and strategies. |
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| How To Increase Productivity With Rapid CIP | Application Note | By Lauren Parker, Jeffrey Cassel, Mike McManaway, and William C. Barrett, Ph.D., W.L. Gore & Associates | This protein capture device demonstration showcases a cycling protocol that uses fast loading and non-loading residence times as well as a rapid CIP out to 100 cycles. |
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DOWNSTREAM MANUFACTURING SOLUTIONS |
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| Connect With Bioprocess Online: |
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