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.