The production of large molecule drugs — such as peptides and monoclonal antibodies — have to meet stringent quality standards in order to ensure their efficacy and safety. To achieve this, both product development and process manufacturing workflows need to be well-designed, tightly controlled, and most importantly, aligned in all handover processes. This is especially important during ‘fill and finish’ (F&F) operations since it’s the last step before the drug is administered to patients.
Given the complexity and inherent instability of most proteins, F&F operations must be designed keeping in mind the environmental factors that can affect their behavior and stability. This raises several challenges for innovation within the biopharmaceutical industry, regarding specialized equipment and processes that ensure the integrity of protein products. On top of this, the move to continuous, fully automated workflows that meet Pharma 4.0 standards is always a consideration.
In this on-demand webinar, Dr. Marcel Tigges from Janssen discusses some of the production challenges faced by researchers working on large molecule process development and how Janssen has optimized their production workflows during F&F by implementing new technologies such as 微量差示扫描荧光技术(nanoDSF). Additionally, Dr. Silvia Würtenberger explains why PR (Prometheus) is the new gold standard that precisely characterizes protein stability.
From watching this on-demand webinar you will:
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