DSG Products — Decentralized and EDC clinical trials

Our user-friendly EDC 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

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.

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.

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.

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.

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.

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.

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.

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.

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.