Enterprise Solutions 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. How Single-Use Technologies Are Simplifying Contamination Control 9/10/2025

    Learn how single-use technologies help reduce contamination risks and support compliance with updated EU GMP Annex 1 guidelines for aseptic processing and sterile drug manufacturing.

  6. Nanoforming Biologics, GLP-1s: From I.V. To Sub Q And Inhaled Delivery 9/9/2025

    Nanoforming enables new delivery routes for biologics and peptides to simplify dosing, enhance patient comfort, and reduce healthcare costs.

  7. Take A Virtual Tour Of Our Cell Line Development Centre Of Excellence 9/8/2025

    Explore the advanced capabilities of our Cell Line Development Center in Ulm, Germany. From expert teams to streamlined processes, discover how we support biopharma innovation.

  8. Benefits Of Outsourcing To An Integrated CDMO 9/8/2025

    Streamlining ADC development through an integrated CDMO can reduce risk and improve quality. Discover why specialized expertise in linker chemistry and bioconjugation is key to overcoming the complexity of ADC manufacturing.

  9. Step Inside One Of America's Leading Protein Biologics CDMO Sites 9/3/2025

    Take a behind-the-scenes look at AGC Biologics’ Seattle campus, one of the most established and productive CDMO facilities in the United States.

  10. Building Quality By Design For Multi-Specific Therapeutic Proteins 9/2/2025

    Platforms incorporating high throughput in silico screening, in vitro expression, and immunosafety of multi-specific molecules can help mitigate potential developability risks and accelerate timelines.