The either-or trap: consequences of enhanced mechanical calibration vs fully qualifying your dissolution equipment

Dissolution and drug release testing are critical to ensuring consistent pharmaceutical performance—but variability in equipment and methodology can introduce serious risk.

In this expert-led webinar, you’ll learn how to:

• Strengthen confidence in your dissolution results
• Minimise variability across batches
• Align with USP expectations for instrument qualification

You’ll also gain insight into the latest advancements in performance verification testing (PVT), including USP’s updated reference standard.

What will you gain by watching? 

• How to ensure reliable and consistent dissolution testing across batches by identifying and controlling key sources of variability
• Why full instrument qualification matters, including the role of both mechanical calibration and performance verification testing (PVT)
• What’s new in USP’s approach, including the scientific rationale and improved sensitivity of the Dissolution Performance Verification Standard (DPVS)

This webinar is designed for professionals involved in pharmaceutical quality, testing, and compliance, including quality control and analytical scientists, pharmaceutical development teams, regulatory and compliance specialists, and laboratory managers responsible for dissolution testing and instrument qualification.