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Three Biotech’s Standardize on BioClinica’s eClinical Suite

Companies complete 42 rapid study starts in 2014

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By: Kristin Brooks

Managing Editor, Contract Pharma

Three mid-sized West Coast biotech organizations have standardized on BioClinica’s  eClinical Suite in 2014. These companies completed 42 rapid study starts last year using a combination of Trident IRT and Express EDC technology in conjunction with BioClinica data management services.
 
The companies used BioClinica’s electronic Case Report Form (eCRF) libraries for study start up that allow reuse of study forms and validated edit checks, and condensing User Acceptance Testing (UAT). These libraries aim to create uniformity and consistency in study builds, data extracts, and reports. 
 
“Using multiple BioClinica products provides advantages in data mapping and reporting,” said John Hubbard, chief executive officer and president of BioClinica. “Combining EDC and IRT, for instance, provides line-of-sight reporting across multiple studies and across programs.” 
 
All three, multi-year agreements include IRT, EDC, and data management and all three organizations are evaluating OnPoint CTMS for enterprise-wide implementation and two are considering the Optimizer clinical trial supply management tool and the Compass intelligent monitoring technology, according to BioClinica.

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