eCaseLink™ EDC

eCaseLink the First Truly Unified Platform

The most successful decentralized or traditional clinical trials begin and end with the highest quality, clean data. The clean clinical data that is collected is in the most streamlined and efficient way possible. Electronic Data Capture (EDC) software is a computerized system designed for the collection of trial data in a electronic format or ECRF that is used in human clinical trials for FDA submission. EDC clinical studies are accomplished with the best clinical trial software, eCaseLink.

The most experienced eClinical provider in the industry, eCaseLink provides study managers and users with intuitive, simple-to-use tools without the need for any programming knowledge. This ensures that any clinical trial is easy, streamlined and best of all, cost-effective.

Speed, efficiency, and accuracy are must-haves for your clinical study. eCaseLink not only meets these critical needs but goes above and beyond to become your ultimate tool for clinical trial success. Our integrated unified software platform enables you to manage your clinical trial life cycle with just one solution provider or gives you the option to “plug and play” with multiple components, giving you flexibility and choice not seen anywhere else.

eCaseLink software features:

  • Remote Randomization
  • Reduce total cost
  • Data integration functionality
  • Rapid, flexible implementation
  • Real-time access to randomization and supply data and reports
  • Customized reporting
  • End-to-end supply chain management
  • Manage randomization & subject enrollment
  • Readiness for risk-based monitoring (RBM)

Additional features:

Protocol Deviations Module – CRAs, Site Users (if requested), and ClinOps may create a new protocol deviation at both Participant and Site level, with review and query workflows, allowing ClinOps or Medical Monitor to request corrections and clarifications required by CRAs.

CaseXPort – FDA-compliant PDF containing all eCRFs for a study, bookmarked and hyperlinked including audit trail, for submission within the eTMF; also, a compliant Site-specific electronic archive for each Site to satisfy records retention requirements.

The benefits of eCaseLink clinical trial software for your study

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 work flow.

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. System development time lines including multiple third-party data integrations average eight weeks.

Comprehensive eSourcing & 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 including: Core, Central, Specialty Laboratory Data, IVRS, CTMS, ECG, CT Scans & MRIs, Topographies & Radiographics, EMR, Medical Device Output, Safety Data.

Complete Reporting

More than 40 standard reports are available as well as a library of configurable standard reports, custom and ad-hoc reports. On-Demand data exports and full ad-hoc reporting enable real-time data access and management.

The highest site acceptance rate

eCaseLink has the highest site acceptance of any EDC system on the market with the most user-friendly interface in the industry. The system is also very flexible and highly configurable. It can adapt to a user’s individual personalized workflow with SmartLinks. SmartLinks automatically adjusts the user interface into a more efficient workspace for each user, based on their unique workflow patterns. Users can easily access a full library of interactive reports at any time, view a snapshot of queries, saved eCRFs, and enrollment, all using eCaseLink’s proprietary dashboard accessible from any screen, making electronic data entry very simple and easy to use.

Multi-language Support

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.

Clear Cost Advantage

DSG offers clients reasonable, straight-forward, cost effective pricing.

Mid-Study Changes in Hours, Not 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.

Global Support

DSG provides 24/7/365 global technical support for all client clinical trial deployments.

Dynamic Integration

eCaseLink is the only electronic data capture solution with dynamic software integration standard.

Datasets on Demand

eCaseLink is the only electronic data capture solution with this feature, standard.