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].

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].

What actions medical device manufacturers could take to strengthen the implementation strategy for EU MDR and IVDR? Recording of 2 days event sessions [15 video sessions].

What is next in testing and analyzing for extractables and leachables in biopharmaceutical development and release? Recording of 2 days event sessions [12 video sessions].