September 28, 2023
Together with professionals in the field, explore the most recent developments in HPAPIs: Containment and Handling. [Recording: 18 video sessions].
March 9, 2023
Learn innovative techniques for analyzing and testing for extractables and leachables in biopharmaceutical development. [Recording: 20 video sessions].
December 1, 2022
Learn about best practices and innovative approaches to manage genotoxic and other mutagenic impurities control strategies. [Recording: 13 video sessions].
September 29, 2022
Explore the latest insights in safe HPAPIs handling together with leading occupational toxicologists and containment experts. [Recording: 15 video sessions].
May 23, 2022
What actions medical device manufacturers could take to strengthen the implementation strategy for EU MDR and IVDR? [Recording: 15 video sessions].
March 30, 2022
What is next in testing and analyzing for extractables and leachables in biopharmaceutical development and release? [Recording: 12 video sessions].
December 2, 2021
Review comprehensive drug impurity profiling strategies in line with regulatory guidelines on new nitrosamine regulations. [Recording: 14 video sessions].
September 29, 2021
Explore how pioneering pharma companies are approaching innovative HPAPI development and processing challenges. [Recording: 12 video sessions].
May 19, 2021
Analytical methods for E&L, regulatory updates & compliance, risk based E&L programs, toxicological risk assessment. [Recording: 13 video sessions].
May 28, 2026
November 5, 2026
December 17, 2026
