Here, we show how Capto™ Q run on an ÄKTA pure™ 25 chromatography system can be used to determine the percentage of full capsids of AAV8 and AAV9 in less than 5 minutes with low sample consumption.
Join viral vector process and analytical development experts as they showcase strategies for developing robust processes and analytics for efficient and de-risked manufacturing.
Build scalable material sourcing strategies for R&D and early phases through to commercialization and learn how to accelerate the development process and ensuring the scalability of your biologics.
Experts discuss the latest strategies for navigating the complexities of cell therapy development and identify clinical development best practices for a successful execution.
Explore a platform that addresses the challenges of on-line nutrient and metabolite monitoring and control.
We outline key updates to the European Pharmacopeia osmolality testing guidelines, analyze their implications for your workflow, and share practical tips to help you navigate the evolving landscape.
In this discussion you will explore the multi-point case for adopting single-use technologies throughout the workflow via an economic, operational, and environmental sustainability lens.
Learn how to build the required data foundations to enable good insights across the BioPharma development lifecycle.
Compare two multimodal resin alternatives used for the polishing step post–protein A capture with data that demonstrates the behavior of multiple mAbs with these two different mixed-mode resins.
Explore data resulting from an initial high-throughput screening experiment carried out to broadly evaluate anion exchange resins that exhibited high LVV recovery.
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