Expert Forum
Best Practices for Updating Analytical Procedures in Drug Development and Manufacturing
Part 1: Overview of Method Life Cycle Management and post-approval changes (17 June, 2025)
Part 2: Practical approaches to implementing new or renewed analytical procedures (24 June, 2025)
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Presenters / Panellists
To be confirmed.
Moderators
Prof. Dr. Cari Sänger-van de Griend
Expert in (bio)pharmaceutical analytical chemistry with 30 years of industrial and academic experience in method development and control strategies, including Analytical Quality by Design (AQbD), and focused on best practices and knowledge sharing.
Dr. Ewoud van Tricht
Expert in (bio)pharmaceutical analysis with over 18 years of industrial experience in analytical development, Quality Control, and Analytical Quality by Design (AQbD). He has contributed to diverse therapeutic modalities, including small molecules, viruses, and cells, at leading companies such as Janssen Vaccines and Sanofi Cell Therapy.
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Contact Us
If you have any questions about the event, don’t hesitate to get in touch with the BioQC Team: Feedback & General Enquiry