Comprehensive, easy-to-use secure clinical trial management software
We offer the most comprehensive, easy-to-use clinical trial management software for any CRO or sponsor in the pharmaceutical, medical device and life sciences industries.
Products — Decentralized and EDC clinical trials
DSG continues to deliver solutions for decentralized and EDC clinical trials.
Efficient online tools and digital resources
We spearheaded the move from paper-based documentation methods to the most effective, efficient online tools and digital resources. Our EDC software is optimized for any clinical trial, academic research or any other research study.
Integrated suite of electronic clinical trial software
Since our founding, DSG has transformed clinical trial data collection and analysis with its integrated suite of electronic data capture software products and solutions for faster ROI and more successful FDA submissions.
Explore our Unified Platform
eCaseLink Designer
Our user-friendly interface gives you complete control to build your study the way you want it, providing flexibility for every type of study.
- Mid-study changes are easily updated without any programming knowledge
- Build databases in less than 2-weeks
- 24/7/365 Global Support
eCaseLink EDC
Offers a user friendly, efficient platform for data entry and data analytics.
- eCaseLink has been instrumental in the approval of multiple blockbuster drugs across various regulatory agencies.
- Real-time data export in any format including SAS.
- Seamless Mid-Study changes without any programming knowledge.
eCaseLink eSource (eClinRO, Direct Data Entry)
Allowing data entry provides a secure, flexible, and convenient approach data capture.
- Empower users to collect data in real-time on any device.
- Designed for decentralized and hybrid research projects.
- Removes the need for SDV.
eCaseLink RTSM (IRT/IWRS)
A streamline fully integrated randomization and trial supply management system with eCaseLink platform.
- Predictive analytics with real-time data to manage supply and re-supply.
- Direct-to-patient drug delivery.
- Rapid, flexible implementation.
eCaseLink eCOA - ePRO (Participant Engagement)
Say goodbye to paper surveys, make it easier for patients to complete questionnaires.
- Enhance global patient engagement with integration of wearables.
- Higher quality patient data with traditional data fields, VAS, and Likert Scales.
- Monitor compliance and analytics in real time.
eCaseLink eConsent
Optimize the Patient Experience & Lower the Barrier to Enrollment.
- Incorporate step-by-step instructions with text, graphics and multimedia options.
- Ability to provide IRB and site-specific consent and reconsent forms.
- Provide participants with engagement activities.
eCaseLink Participant Tracker
Meet your enrollment goals with a comprehensive platform to track pre-screened participants.
- Pre-screen potential participants for more efficient and accurate enrollment workflows.
- Provides better control of recruitment by monitoring subjects being registered.
- Offer participants with engagement activities.
eCaseLink TeleHealth
Empower your sites and investigators to communicate with participants anywhere.
- Better patient engagement and reduces the burden of travel time.
- Facilitate meaningful dialog without the need for on-site visits.
- Capture clinical outcome assessment (COA’s) remotely.
eCaseLink Safety
Easy tool for Pharmacovigilance to keep track of Safety events and helps report to regulatory bodies.
- Track safety events across study protocols and generate reports.
- Privilege based workflow with multi-level approval.
- Generate FDA submission forms with safety data auto populated.
eCaseLink CTMS
Provides unparalleled control over your study with advanced reporting, protocol deviations, workflow events, and more.
- Track studies across the divisions of multiple sponsors.
- Payments module includes budget-versus-payment and time-phased reporting.
- Comprehensive investigator database includes status, categories, office locations, personnel, and credentials.