Catalent Biologics Content
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Catalent Capacity Update April 2025: Fill/Finish
4/25/2025
This presentation highlights how simplified execution with development, filling, and analytics under one roof ensures safe, efficacious products reach patients in need.
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Mastering QbD For Successful Process Validation Campaigns And Commercial Manufacturing Of Biologics
2/18/2025
In this presentation, industry-leading bioprocess experts explore the challenges and opportunities that arise when implementing Quality by Design (QbD) in biologics development and manufacturing.
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Formulation Through Manufacturing Under One Roof
2/18/2025
Partner with a CDMO that understands the unique challenges of emerging biopharma, providing expert guidance in formulation development, manufacturing, and regulatory navigation.
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High-Throughput Preformulation Development Platform For Biologics
11/21/2019
A high-throughput formulation development for sample preparation and sample analysis enabled a simple and less labor-intensive screening of a broad range of conditions in considerably less time.
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Strategies To Achieve Successful Approval And Launch
11/18/2019
Four experts share how scale-up, regulatory expectations, demand forecasting, and process validation all play a role in the success of a biologic when embarking upon the commercial manufacturing journey.
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Ensuring Success In Early Biopharmaceutical Formulation Development
6/10/2019
Biopharmaceuticals tend to be highly unstable. A pilot formulation study at the early drug substance development stage can make things considerably easier at the manufacturing stage.
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High-Throughput Formulation Development For High-Concentration mAbs
6/10/2019
How a high-throughput, microwell plate platform can be used to economically screen a model IgG1 mAb at 120 mg/ml in 96 formulations while minimizing protein consumed and generating large amount of data.
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Achieving A Successful Drug Product Technology Transfer
Get insights on key considerations for a successful process transfer for manufacturing a drug product, including a case study on overcoming challenges in a process transfer for a sterile diluent.
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Getting Your Biologic To Clinic Faster & More Efficiently
There are a range of benefits to use an integrated supplier to streamline biologic drug development starting in early phase through clinical and commercial stages.
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European Center Of Excellence For Clinical Biologics
Explore how our proven expertise and simplified execution with development, filling, and analytical under one roof ensure safe, efficacious products reach patients in need.