Cell and Gene Outsourcing
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Revolutionizing How Medicines Are Made, Funded, And Scaled
5/9/2023
Hear from site leaders and virtually tour the process and analytical development laboratory and GMP manufacturing facility which includes four additional 2,000L single-use bioreactors.
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Scalable Suspension LVV Production Platforms
Review a scalable suspension-based Lenti production platform using a proprietary HEK293T clonal cell line and improvement steps to generate commercially viable therapies from concept to patient.
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Identify And Quantify AAV Fill States Using Analytical Ultracentrifugation
3/14/2024
Explore how to implement analysis using sedimentation velocity analytical ultracentrifugation to characterize AAV size distributions and multiple detection wavelengths to identify various fill states in AAV preparation.
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Cell & Gene Therapy Development: Characterization Of Cellular Starting Material
6/21/2024
Watch to gain valuable insights into the characterization of cellular source material for the development and manufacture of cell and gene therapy-based products.
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Meeting Needs And Exceeding Expectations Worldwide
10/16/2024
Whether you are looking to optimize your existing formulations or require full-scale manufacturing solutions, Boehringer Ingelheim BioXcellence™ is dedicated to helping you realize your vision and deliver impactful therapies.
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Candidate Screening And Feasibility Studies For Viral Gene Therapies
Create a simple, modular path to cGMP manufacturing that minimizes risk. Explore a strategic approach for early-stage development and how it can propel therapies to the clinic and the market.
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Early Preclinical Development: A Successful Transition To cGMP Manufacturing
12/2/2024
Explore the development steps that lead to an mRNA construct optimized for your requirements and that meets future-proof cGMP manufacturing requirements, thereby de-risking the development.
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Combining An MVA Technology Platform With Innovative Analytical Methods
7/21/2023
Learn how this process development platform for MVA impacts vaccine manufacturing and supports the drug life cycle from process and analytical development through trials and commercialization.
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Secure And Industrialize Your CGT Process Towards cGMP Manufacturing
Learn the principles of commercialization readiness and guidance to address them in process development as well as the best time to implement automation and minimize commercialization risks.
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Sustainable Approaches To Oligonucleotide Manufacturing
An industry expert shares about sustainable Oligo manufacturing approaches that can save time, cost, and resources – while improving purity, quality, and scalability of these promising therapeutics.