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Clinical Data Repository

Data is the crown jewel of Bio-Pharma companies yet many companies put the data received from a CRO on a CD in a drawer or file the SAS datasets somewhere. Companies do not leverage their clinical data. By standardizing data across clinical trials using a CDISC compliant data standards global library, capturing the data via EDC, and transferring into a Clinical Data Repository you not only increase operational efficiencies, you have the ability to:

  • pool data across Phases,
  • look at safety data across products,
  • use a review tool across pooled data to analyze data trends,
  • use data mining for personalized medicine and targeted populations,
  • allow staff to oversee and manage clinical trials through a single user interface with role-based access,
  • get rapid, near real-time access to data on clinicians' desktops,
  • respond to regulatory authority questions quickly and confidently,
  • use data to make go/no-go decisions in product development,
  • look for data trends on marketed products for best practices in patient care, and
  • give access to investors and clinical development partners to make business decisions.

Expert eClinical Solutions staff can build a clinical data repository, convert legacy data, and manage your clinical data ongoing.

Learn about all of our delivery models.

NEWS & EVENTS

03/20/09
eClinical Solutions Senior Manager Presents at SAS Global Forum 2009

03/12/09
Eliassen Group President Joins NACCB Board of Directors

03/06/09
eClinical Solutions' Senior Managers Offer Two Presentations at the 24th Annual DIA Data Conference and Exhibition