Our capabilities include clinical strategy development, identification of study populations and clinical data required for product claims, prospective specimen collections, and biospecimen acquisitions.
Trial and data integrity are assured and managed utilizing our Electronic Data Capture (EDC) and Clinical Trial Management System (CTMS) applications.
Clinical study execution includes the internal and external validation testing, clinical sample testing and the reproducibility of results.
Fujirebio also maintains an extensive biospecimen bank with over 50,000 samples managed through our Laboratory Information Management System (LIMS), which assures samples are of the highest integrity.
Contact us about your CDMO project
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