In this issue experts explore the development of targeted protein degradation drugs, how potential legislative changes may impact the EU and selecting the right downstream process for bi-specific antibodies. Also featured in this journal, how RMM can enable efficient shutdown recovery, five critical areas for data integrity in life sciences and so much more!
Included in this issue:
EVENT REVIEW European Pharmaceutical Review’s The Future of Bio/Pharmaceutical Analysis Online Summit
QA/QC Microbiology/RMM Testing non-inferiority for accuracy of quantitative microbiological methods
Edwin van den Heuvel and Maliheh Heidari, Eindhoven University of Technology, Kathrin Möllenhoff, Heinrich-Heine-University, and Pieta IJzerman-Boon, Center for Mathematical Sciences
MANUFACTURING The importance of sterility testing in biopharmaceutical manufacturing
Thermo Fisher Scientific
VACCINE DEVELOPMENT Anatomy of a ‘correlate of protection’ for T-cell vaccines
Thomas Rademacher, Emergex Vaccines
HPAPI The challenge of handling highly potent API and ADCs in analytical chemistry
Elodie Barrau and Olivia Jones, Eurofins
GUIDE TO: Data Integrity Reducing human error with better technology
Drug Development Global Blood Therapeutics: driving innovation in sickle cell disease
Sebastian Stachowiak, Global Blood Therapeutics (GBT)
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