It's two-day virtual event focused on the latest developments, regulatory expectations and technical challenges in genotoxic impurity control.

Gain insights into the latest techniques for testing and analyzing Extractables and Leachables. Access full recordings of all sessions from the two-day event.

What are critical considerations on drug-device integrated development and how to choose the right regulatory and clinical strategy?

How to better adapt smart manufacturing in pharma and boost the opportunities offered by emerging technologies?