Clinical Trial Biospecimen and Consent Tracking

Learn about the BioFortis solution for addressing new challenges around sample and consent tracking

Clinical trials today involve sophisticated sample collection and analysis. Samples are tested to generate scientific data in order to determine patient segmentation and to demonstrate efficacy and safety of the drug under study. In addition, samples, with proper consent, can also be used to provide researchers with greater insights into biological pathways and related diseases in future studies. 

Complete the form below to access this white paper