Analytical Development and Quality Control teams often approach assays from very different angles – innovation and flexibility on one side, reproducibility and compliance on the other. The challenge is making sure methods can travel smoothly between both worlds without losing robustness or reliability. 

Join to:

• Understand why methods developed flexibly in AD often struggle in QC – from reliance on new technologies and reproducibility – to ensure assays remain reliable when moved into regulated testing environments
• Building strategies to adapt and validate assays for QC environments to secure regulatory compliance, enable timely batch release, and prevent costly delays
• Overcoming site-to-site variability with platformization principles to streamline method transfer, reduce revalidation burden, and accelerate readiness from development to QC and commercial release