A premier two-day event dedicated to best practices, regulatory expectations and emerging trends in pharmaceutical cleaning validation.

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

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?

Stay updated on industry trends, improve product quality and ensure safety in parenteral drug manufacturing. Recording of 2 days event sessions [15 video sessions].

This event to learn about the latest methods for testing and analyzing Extractables and Leachables. Recording of 2 days event sessions [16 video sessions].

Meeting with subject matter experts to evaluate different points of view on how to solve the problems associated with mutagenic impurities. Recording of 2 days event sessions [13 video sessions].

Looking to build compliant cleaning validation program and ensure that your next product is not affected by contamination? Recording of 2 days event sessions [14 video sessions].

What is next in testing and analyzing for extractables and leachables in biopharmaceutical development and release? Recording of 2 days event sessions [18 video sessions].