Manufacturing Logistics Webinars

1. The Interoperability Challenge In Single-Use 9/12/2025

   In this segment from the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” our panelists define the main challenge plaguing single-use users: a lack of standards across systems and components. This absence of standardization creates a demand for deep, system-specific expertise that complicates interoperability across the industry and even within an organization. They discuss the many layers of nuance and complexity that make large-scale standardization difficult.

2. Addressing Mismatched Connectors And Overcoming Validation Hurdles 9/12/2025

   During the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” audience members indicated mismatched connectors and validation challenges as their biggest pain points. In this segment, our panelists respond to the audience and weigh in on how to mitigate these difficulties.

3. Planning For Flexibility And Supply Chain Resilience 9/12/2025

   In this segment from the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” our panelists discuss the importance of working with your quality team to plan for flexibility, a lesson the industry learned the hard way during the COVID-19 supply chain disruptions.

4. Single-Use Standardization Starts Internally 9/12/2025

   We've all heard the expression: If you want to change the world, start at home. Single-use standardization is no different. In this segment from the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” our panelists Mark Petrich, Ph.D., and Frank Gillam, Ph.D., reflect on their success and struggles standardizing single-use systems within their respective organizations.

5. Developing An In Vivo CAR-T With Interius BioTherapeutics' Sianny Christanti and Babu Medi, Ph.D. 8/12/2025

   On this episode of Better Biopharma, Interius BioTherapeutics’ Sianny Christanti and Babu Medi, Ph.D., explain how the company is re-engineering a lentiviral vector to enable INT2104, its off-the-shelf, in vivo CAR T-cell therapy. They discuss the vector's design and its manufacturability, as well as the analytical and regulatory challenges of bringing this first-in-human therapy to the clinic.

6. Secure Your Sensitive Drug Substances 8/7/2025

   Explore the risks of freeze and thaw cycles on biological products and how an advanced plate freezing platform protects sensitive molecules with precision and ease.

7. Unlocking The Cold Chain Of Proteins 7/3/2025

   Discover how controlled freezing minimizes cryoconcentration and protein denaturation in bulk drug substances. Learn about efficient, scalable freezing solutions for enhanced product stability.

8. Navigating The New USP Chapter <382> For Elastomeric Closures 6/24/2025

   Dive into the scope of <382> for pharmaceutical closures and the regulatory landscape. Learn about new required tests and instrumentation for compliance and recommendations on method implementation.

9. BPI Interviews Purification And Pharma Analytics Leader 6/9/2025

   Jean Luo, VP of Purification and Pharma Analytics, discusses innovations in bioprocessing, including the development of dPCR assays, lentiviral titer systems, chromatography resins, and supply chain.

10. Ultralow Particulate Bottles And Carboys: Where Being Particular About Particulates Is Critical 5/27/2025

    Optimize your operations with ready-to-use, meticulously prepared containers. Learn how our commitment to cleanliness reduces risks and supports your most critical requirements.