eCaseLink™ EDC

eCaselink EDC delivers streamlined studies, clean data, and results.

eCaseLink™ combines novel technology and unmatched industry experience to help Reduce clinical trial time, improve accuracy, drive down costs/improve ROI, prevent risk, and use clinical trial data more effectively.

The most successful clinical trials begin and end with the highest quality, clean data. Data that is collected in the most streamlined and efficient way possible. The most successful studies are accomplished with eCaseLink EDC.

eCaseLink EDC consistently delivers clean data, quick and efficient workflow, accelerated reporting and analysis, rapid database lock, and faster FDA submission and acceptance—resulting in high ROI.

DSG's eCaseLink technology is unique. A proprietary, user friendly-interface and instant data validation accelerate data collection and ensure consistent, high quality data in real time.

Please request an online demo of eCaseLink today and take an important step toward achieving your most successful clinical trials.

• Instant Validation
  eCaseLink’s proprietary technology validates information field-by-field, instantly-without connecting to the server or requiring client plug-ins. Instant validations decrease the number of times the user must submit a form and the amount of bad data that must be queried after a submission. When you save a page, you are saving a page of clean data. The result is cleaner data and a rapid workflow.
• High site acceptance
  eCaseLink’s user interface is unique. The eCRF data entry screens are identical to paper CRFs, providing a look and feel that’s very familiar to site users. Combined with a user-friendly interface, eCaseLink makes electronic data capture easy and efficient.
• Clear Cost Advantage
  DSG offers clients reasonable, straight-forward, cost effective pricing.
• Rapid EDC Study Start-Ups
  eCaseLink's page-based technology allows for rapid set-up, testing and deployment of the first several visits of a study without delay, so there's no need to wait for the EDC team to create validation edits. Library eCRFs are saved and re-used, affording faster trial set-up for future studies. eCaseLink allows for setups in as little as 2 weeks.
• Mid-Study Changes in hours, instead of weeks
  eCaseLink allows you to manage protocol amendments and any mid-study changes quickly and seamlessly without any system downtime.
• Local Lab Management System
  eCaseLink enables data managers to effectively manage local labs and normal lab ranges, and also provides interactive review of laboratory data.
• Comprehensive eSourcing and Integration
  Data integration functionality allows users to integrate and manage data from a wide variety of industry sources in a single database with convenient dashboards for viewing and accessing data
  • Core, central, specialty laboratory data
  • IVRS
  • CTMS
  • ECG
  • CT Scans & MRIs
  • Topographies & Radiographics
  • EMR
  • Medical Device Output
  • Safety Data
• Robust Reporting
  More than 40 standard reports are available as well as a library of configurable standard reports, custom and ad-hoc reports. SAS On-Demand Exports and full Ad-Hoc Reporting enable real-time data access and management.
• Multi-language
  eCaseLink multi-language capabilities include Japanese, Chinese and Western European languages to support trials worldwide. This allows sponsors to run their clinical trial operations on a single, global platform without needing to install different versions of the software for different languages. Additionally, data managers and clinicians can work together collaboratively using a single, centrally-managed global database regardless of geographic location or language.
• Dynamic integration
  eCaseLink is the only electronic data capture solution with this feature, standard.
• SAS Datasets on Demand
  eCaseLink is the only electronic data capture solution with this feature, standard.

eCaseLink™, DSG's ground-breaking electronic data capture (EDC) software application, was one of the first successfully deployed Electronic Data Capture software applications on the market. It was developed in 1999 to provide robust, clean data analysis for one of the world's top pharmaceutical corporations. Since then, eCaseLink has been deployed in over 1,000 clinical trials for more than 325 companies, at over 18,000 sites in over 68 countries. It provides instant data analysis at the field level, without the need to submit to a server.

eCaseLink™   |   Winner of the 2007 and 2008 SCDM Data Driven Awards