Related events as part of the webinar series
Register now:
- Moving HCP LC-MS analysis into a GMP environment – coming!
- Advanced ELISA-MS™ for Host Cell Protein (HCP) ELISA Antibody Characterisation – coming!
Expert Forum
Regulatory expectations for your HCP analysis: meet USP <1132.1> to enhance the quality of MS-based data
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Presenters / Panellists
Ejvind Mørtz, PhD
Co-Founder & COO
Alphalyse (Denmark)
Ejvind holds a PhD from the University of Southern Denmark in Protein Chemistry & Molecular Biology. He has more than 20 years of experience developing protein analyses and mass spectrometry methods in the research & development of protein biologics, vaccines, monoclonal antibodies, therapeutic proteins, and cell and gene therapies.
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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