eCaseLink – the DCT and Clinical Trial Platform.
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eCaseLink the First Truly Unified Platform
Secure clean data
The most successful decentralized or traditional clinical trials begin and end with the highest quality, clean data. 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. The most efficient and streamlined way to collect and capture clean clinical trial data is only accomplished when using the best clinical trial software in the industry, eCaseLink.
Simple cost-effective integration
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
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 EDC software features:
- Easy to use, and loved by users
- Rapid setup
- Guided workflow
- Comprehensive full service, and efficient self-service
- Supports mobile use – eSource and home visit data collection
- Supports remote SDV
- Supports complex study designs
- Part of a broader, unified product suite including eConsent, eCOA, RTSm and more
- Delivered with attentive project management
Additional Modules:
Protocol Deviations – 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 – Generates an FDA-compliant Site-specific electronic archive PDF containing all eCRFs used for a study that are bookmarked and hyperlinked including an audit trail, for submission within the eTMF; for each Site to satisfy records retention requirements.
Learn how the eCaseLink platform works
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 a very high site acceptance 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
No Study is to big or to small. 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 has dynamic software integration standard.
Datasets on Demand
eCaseLink provides datasets on demand as a standard feature.