![Modernizing Pharmaceutical QC Laboratories From Locked Data to AI‑Powered Decisions [Jon Welsh]](https://cdn.podme.com/podcast-images/5CED7BB7C445808AA9E69B5517680A37_small.jpg)
Modernizing Pharmaceutical QC Laboratories From Locked Data to AI‑Powered Decisions [Jon Welsh]
Imagine unlocking 20 years of QC data to let AI forecast instrument downtime. John Welsh of Agilent reveals how the Allotrope simplified model and modern lab informatics turn compliance into a competi...
22 Sep 39min

Reducing Risk and Costs: Continuous Water Quality Monitoring in Pharmaceutical Production
In this episode, Yan Kugel and Konrad Sägesser discuss the latest trends and practical solutions in pharmaceutical water quality monitoring. Learn how continuous analytics, compliance, sustainability,...
31 Aug 33min
![Overcoming Tech Transfer Bottlenecks: From Paper Trails to Standardized Digital Hubs [Nikki Bishop]](https://cdn.podme.com/podcast-images/5CED7BB7C445808AA9E69B5517680A37_small.jpg)
Overcoming Tech Transfer Bottlenecks: From Paper Trails to Standardized Digital Hubs [Nikki Bishop]
Can a single click replace years of tech transfer paperwork? Nikki Bishop, VP of Marketing & Experience at Emerson , reveals how AI‑driven digitization could slash delays for pharma, biotech, med‑tech...
25 Jun 51min
![Transforming Pharmaceutical Development with Active Packaging [Badre Hammond]](https://cdn.podme.com/podcast-images/5CED7BB7C445808AA9E69B5517680A37_small.jpg)
Transforming Pharmaceutical Development with Active Packaging [Badre Hammond]
Can custom active‑packaging technology add three years to a drug’s shelf life?Badre E. Hammond, Global VP of Aptar Active Material Science, reveals how early‑stage material science can slash developme...
4 Jun 44min

How Process Analytical Technology Moves Quality into Real Time - Stanislav Kasakov
Process Analytical Technology (PAT) has evolved from a niche troubleshooting tool into a strategic necessity—but most companies still implement it too late. Dr. Stanislav Kazakov from Thermo Fisher S...
13 Mai 57min

Driving Global Quality in Viral Vector Manufacturing with Melanie Kearney
What does it take to keep pharma & biotech CDMOs inspection‑ready across global sites? Senior VP of Global Quality, Melanie Kearney, reveals how she transforms quality culture, bridges R&D and manufac...
29 Apr 55min
![Agility in Pharma: Transforming Challenges into Opportunities [Elizabeth Hickman]](https://cdn.podme.com/podcast-images/5CED7BB7C445808AA9E69B5517680A37_small.jpg)
Agility in Pharma: Transforming Challenges into Opportunities [Elizabeth Hickman]
Yan Kugel is joined by Elizabeth Hickman, the CEO at AustinPx. With over a decade of experience in the biotech and pharmaceutical sectors, Elizabeth shares her insights on drug development, innovative...
26 Nov 202433min
![Risks and Rewards in GMP Process Automation [Will Moss] #77](https://cdn.podme.com/podcast-images/5CED7BB7C445808AA9E69B5517680A37_small.jpg)
Risks and Rewards in GMP Process Automation [Will Moss] #77
In this episode, Yan Kugel is joined by Will Moss founder and CEO of Seal, about the critical need for automation in GXP processes. Will shares his expertise on balancing automation with human oversig...
3 Sep 202443min


















