Facility Design Webinars

1. Lessons From FDA 483s And Warning Letters: Cleanroom Compliance 12/8/2025

   Learn critical lessons from FDA 483 observations and Warning Letters to proactively address common GMP cleanroom compliance failures and build an inspection-ready facility.

2. Optimizing Monitoring: The Science Of Particle Loss 11/26/2025

   Explore how tubing configuration impacts particle recovery and compliance under Annex 1, using evidence-based guidance, risk assessment tools, and practical strategies to strengthen contamination control.

3. Streamlining pDNA: Capacity, Complexity, And Cutting-Edge Solutions 11/20/2025

   Learn how flexible facility design and process innovation are accelerating pDNA manufacturing, as well as key strategies to avoid scale-up pitfalls and meet growing therapeutic demand.

4. Lessons In Scaling Regenerative Medicine Manufacturing With Organogenesis's Patrick Bilbo 11/18/2025

   In this episode of "Better Biopharma," Tyler Menichiello is joined by Patrick Bilbo, chief operating officer at Organogenesis, a regenerative medicine company developing and manufacturing advanced wound care products.

5. Automated Bioburden Testing Solution 11/7/2025

   Automation is transforming microbial quality control labs, boosting productivity, minimizing errors, and ensuring data integrity. Discover how digitalization is driving Pharma 4.0 and reshaping lab workflows.

6. Cell Culture Media Manufacturing, Paisley, Scotland 11/4/2025

   Learn more about our cell culture media manufacturing global network, including details of the Paisley, Scotland site's capacity expansion supporting the bioprocessing industry's rapidly growing needs.

7. Cell Culture Media Manufacturing, Grand Island, NY 11/4/2025

   Learn more about our cell culture media manufacturing global network, including details of the Grand Island, New York sites capacity expansion supporting the bioprocessing industrys rapidly growing needs.

8. 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.

9. Supplier Standards And Building Hybrid Single-Use Models 9/12/2025

   In this segment from the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” the panelists advise taking a unit operations approach to standardization. They also emphasize the growing trend of the plug-and-play hybrid models in single-use.

10. How End Users Can Drive Single-Use Harmonization 9/12/2025

    Though progress has been made in supplier-created standards, broader harmonization is difficult to balance in a competitive supplier market. In this segment from the Bioprocess Online Live event, “Single-Use Harmonization Needs A Tune Up,” the panelists encourage self-regulation for the industry. This bottom-up approach, where standardization begins with end users, will ultimately put competitive pressure on suppliers.