Save your seat for our solution-packed webinar to be equipped with best practices and novel approaches to control genotoxic and elemental impurities.

What is next in testing and analyzing for extractables and leachables in biopharmaceutical development and release?

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?

Explore the latest insights in HPAPIs handling together with industry leaders, occupational toxicologists and containment experts

What actions medical device manufacturers could take to strengthen the implementation strategy for EU MDR and IVDR?

What is next in testing and analyzing for extractables and leachables in biopharmaceutical development and release?

Save your seat for our solution-packed webinar to be equipped with best practices and novel approaches to control genotoxic and elemental impurities.

Explore the latest insights in HPAPIs handling together with industry leaders, occupational toxicologists and containment experts