Looking to build compliant cleaning validation program and ensure that your next product is not affected by contamination?

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?

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].

Learn the best techniques and cutting-edge methods for reducing genotoxic and elemental impurities. Recording of 2 days event sessions [17 video sessions].

Together with professionals in the field, explore the most recent developments in HPAPIs: Containment and Handling. Recording of 2 days event sessions [18 video sessions].

Learn innovative techniques for analyzing and testing for extractables and leachables in biopharmaceutical development. Recording of 2 days event sessions [20 video sessions].

Learn about best practices and innovative approaches to genotoxic and other mutagenic impurities control. Recording of 2 days event sessions [13 video sessions].

Explore the latest insights in HPAPIs handling together with occupational toxicologists and containment experts. Recording of 2 days event sessions [15 video sessions].