Related Experiment Video
Updated: Aug 7, 2026

06:37
Using Reference Reagents to Confirm Robustness of Cytokine Release Assays for the Prediction of Monoclonal Antibody Safety
Published on: September 15, 2023
Counterpoint: Food and Drug Administration guidance for C-reactive protein assays: matching claims with performance
James V Callaghan1, Steven I Gutman
1Office of In Vitro Diagnostic Device Evaluation and Safety, Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD 20850, USA. james.callaghan@fda.hhs.gov
Clinical Chemistry
|June 27, 2006
Abstract
No abstract available in PubMed .
