Outsourced Pharma Webinars
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Quality Roundtable: Optimizing Biologics Manufacturing Processes With Raw Materials
1/24/2024
Improve your commercial manufacturing process with advice from regulatory and raw materials experts on the development journey from pre-clinical to licensure.
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Manufacturing Solutions Using Hard-Shell, Liquid-Filled Capsules
1/11/2024
Discover the advantages of LFHCs, including improved solubility and bioavailability, enhanced stability, and customizable release profiles, and how they can accelerate drug development timelines.
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Overcoming Challenges Of Manufacturing For Clinical Trials
1/11/2024
Learn how CROs and CDMOs work in tandem to address operational and regulatory challenges for pharmaceutical and biotech companies, and how this can determine study success or failure.
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Developing Nanosuspension Formulations For Poorly Soluble Drugs
1/11/2024
Learn more about the benefits of nanomilling, types of milling media and stabilizers, and scale up for clinical manufacturing.
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Leveraging Stable Pool Material To Expedite The Path To IND
1/10/2024
Review the efficacy of fast stable pools in generating purified product at an early stage and learn how to accelerate the journey toward first-in-human trials and proof-of-concept studies.
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Optimization-By-Design - A Critical Factor In Viral Vector Scale Up
12/14/2023
Learn how leveraging the expertise and capabilities of an experienced partner is a key factor in optimizing AAV processes using Design of Experiment (DoE), thereby reducing variability and risk.
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Upstream To Downstream: A Comprehensive Approach To AAV Production
12/7/2023
How can you face the challenges of AAV production, scale up your AAV manufacturing effectively, and enhance the recovery and purity in your downstream processing.
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Harnessing New Tech To Create Next-Generation GS-CHO Expression Solutions
12/6/2023
What makes a next-generation CHO bioproduction process? Take a journey through areas of innovation for creating expression systems of the future, with a focus on DNA and cell expression technologies.
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Nitrosamine Impurities Deadline: Are Your Products Compliant?
12/5/2023
Learn how to select an experienced nitrosamine mitigation provider and how a tailored, quantified strategy can help you bring your product into compliance while maintaining control of the process.
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Reaching BLA Success: Fast-Track Approach To Process Characterization
11/30/2023
Discover how knowledge of microbial processes and process characterization understanding can be used to design targeted BLA programs while managing risks.