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Regulatory expectations for your HCP analysis: meet USP to enhance the quality of MS-based data

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Regulatory expectations for your HCP analysis: meet USP <1132.1> to enhance the quality of LC-MS-based dataEjvind Mørtz, PhD

Panel Discussion

Presenters / Panellists

Presenters / Panellists
Ejvind Mørtz, PhDCo-Founder & COOAlphalyse (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.
Derrick ZhangSenior Scientist IIUS Pharmacopeia (USA)
Eef DirksenDirector Analytical Development and Quality ControlByondis (Netherlands)

Moderators

Moderators
Dr. Ewoud van TrichtScientific DirectorBioQCExpert 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.
Prof. Dr. Cari Sänger-van de GriendScientific DirectorBioQCExpert 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.

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