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Three West Coast Biotechs Standardize on BioClinica

– Multi-Million Dollar, Multi-Year eClinical Deals Signed in 2014 –

January 22, 2015

NEWTOWN, PA, JANUARY January 22, 2015 – BioClinica®, Inc., a leading provider of outsourced clinical trial services and eClinical technologies, reported today that three mid-sized West Coast biotech organizations standardized on its eClinical Suite in 2014. These biotech 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 number of studies launched is expected to climb substantially in coming months.

These and other life sciences companies have standardized on BioClinica's eClinical Solutions for the efficiencies surrounding data management and the value of highly connected data. "Using multiple BioClinica products provides advantages in data mapping and reporting," said John Hubbard, CEO and President for BioClinica. "Combining EDC and IRT, for instance, provides line-of-sight reporting across multiple studies and across programs."

Accelerated study start up times have been achieved with the aid of electronic Case Report Form (eCRF) libraries created by BioClinica. These libraries allow reuse of study forms and validated edit checks, condensing User Acceptance Testing (UAT) while creating uniformity and consistency in study builds, data extracts, and reports. Such benefits are especially attractive to growing research organizations with developing programs where new personnel must get up-to-speed quickly.

BioClinica offers mid-sized and start up biotech companies a unique value proposition. "From unlimited imports and on-demand exports to linked query and data listings to seamless integrations, our technology solutions take the customer from Phase I through pivotal trials and beyond while providing the most sponsor friendly business model in the industry," Hubbard said.  It also supports growth in a more controlled way as an organization is able to focus hiring in clinical operations to manage sites and oversee monitoring activities while leaving data management to BioClinica.

The key advantage to our unique sponsor-friendly business model is our predictable pricing and unmatched support. "BioClinica customers only pay for the software they need and when they need it," Stephen Boccardo, BioClinica SVP of eClinical Business Development said. "With our extensive in-house clinical trial expertise BioClinica is viewed as an extension of our sponsors' teams rather than a vendor to be managed and monitored."

All three agreements under the multi-million dollar, multi-year deals include IRT, EDC, and data management.  In addition, all three biotech 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.

To request a meeting with BioClinica to learn more about our eClinical Solutions or to schedule a product demonstration, call our hotline at 1-888-392-7456, email or complete the online Contact Us form. Follow BioClinica on the Trial Blazers blog at, and on Twitter at

About Bioclinica

Bioclinica is a global life sciences solution provider that utilizes science and technology to bring clarity to clinical trials – helping companies to develop new life-improving therapies more efficiently and safely. Successful clinical trials require the ability to see key details and uncover hidden insights, and Bioclinica’s hundreds of experienced scientific, medical, and domain experts bring unmatched insight across the development lifecycle, from the initial protocol to post-approval.  The company’s cloud-based offerings include medical imaging; cardiac safety; clinical adjudication; randomization and trial supply management and optimization; electronic and eSource data capture; site payments and forecasting; pharmacovigilance; trial management; and risk-based monitoring solutions. A true multifaceted partner to trial sponsors and Contract Research Organizations (CROs), Bioclinica offers an integrated App xChange partner ecosystem, a global network of research sites, patient recruitment services, and post-approval research expertise to provide committed, detail-focused service through all stages of drug development.  The company’s thousands of employees serve more than 400 pharmaceutical, biotechnology and device organizations – including all of the top 20 biopharmaceutical companies and leading CROs – through a network of offices in the U.S., Europe, and Asia.

Learn more about Bioclinica and our Clinical Adjudication and other offerings at and in the Bioclinica Blog. Follow the latest company news and happenings on LinkedIn and Twitter.


Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

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