Analytical And Quality Control
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Interview With Pharma Analytics Field Application Specialist - Sandi True
11/6/2025
Hear Sandi True, a Field Applications Specialist discuss helping customers navigate challenges often encountered when evaluating and implementing Residual DNA Quantitation, Mycoplasma Detection, and Microbial Identification Assays.
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Digital Solutions For Accelerated Innovation
5/19/2025
In this webinar, hear how Applied Biosystems AccuSEQ software serves as an advanced digital tool that can help streamline bioanalytical processes and accelerate the delivery of life-changing therapies.
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Leveraging dPCR r Techniques To Quantitate Lentivirus Particles
5/28/2025
Discover how digital PCR can streamline lentiviral vector characterization to reduce variability and improve analytical sensitivity. Learn how this approach can help you comply with regulatory guidance.
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Next-Gen Disease Models And Cell Therapeutics: Innovations In AI, Omics And Collaboration
8/20/2025
Learn how to leverage AI, omics integration, and collaborative research to build more physiologically relevant disease models and accelerate the development of next-gen cell therapies.
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Advancing Vaccine Development With Novel Chromatography Solutions & Quality Testing
6/24/2025
Learn more on novel chromatography solutions that can help improve the downstream processes of different vaccine types such as mRNA, recombinant proteins, and Virus-Like Particles (VLPs).
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Applying AI And Rapid Prototyping To Media And Process Development
3/26/2026
Hear from industry experts on how teams can integrate manufacturability considerations earlier through rapid prototyping, data-driven media development, and predictive modeling.
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Rapid Process Development And Technical Support For AAV Scaleup
12/17/2024
Accelerate your AAV production journey. Learn how rapid process development and expert support can streamline your path from vial to purified bulk, ensuring scalable and efficient manufacturing.
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A Successful Journey To Cell Therapy Manufacturing
5/29/2025
Learn about the three main areas to consider when you're preparing to commercialize a cell therapy, including starting/raw material, the controlled manufacturing process, as well as testing safety and quality.
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A Straightforward Path Toward Regulatory Compliance & Data Integrity With Your Microbial Testing Systems
11/10/2025
In this webinar, we will share a variety of strategies for implementing and validating microbial identification systems in the cGMP environment, possible difficulties along the way, and a comprehensive solution that addresses these challenges.
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Innovations In Mycoplasma And Sterility Testing For Biopharma
5/22/2025
In this webinar, our expert speakers will discuss the types of analytical testing that can be effectively employed in the early stages of therapeutic development and subsequently scaled to meet production challenges.