DSG - Clinical Trial Software and Data Management Services
DSG continues to deliver the most comprehensive, easy-to-use clinical trial management software for any CRO or sponsor in the pharmaceutical, medical device and life sciences industries.
We spearheaded the move from paper-based documentation methods for clinical trials to the most effective, efficient online tools and digital resources. Since our founding, DSG has transformed clinical trial data collection and analysis with its integrated suite of electronic data capture software products and innovative solutions for faster ROI and more successful FDA submissions.
DSG offers a full range of DSG eClinical software and Data Management services
eCaseLink Designer™
Tech Transfer - eCaseLink Designer lets the user become the creator with complete control of a streamlined eCRF workflow. DSG’s unparalleled clinical support services and hands-on training ensure that you build studies end-to-end for a successful clinical trial execution. We help you create reusable templates, customized eCRFs that can lower cost to deliver a completed study for FDA regulatory approval.
eCaseLink™ EDC
eCaseLink is an award winning web based electronic data capture software application that enables the most advanced clinical data collection while still providing an easy-to-use, user-friendly presentation of eCRFs. eCaseLink provides the fastest start-up time, clean data, and rapid database lock, that will only result to more successful FDA submissions, resulting in a greater ROI.
eCaseLink IRT
DSG’s award winning IRT (Interactive Response Technology) is a seamlessly integrated component of eCaseLink that helps you to easily manage randomization, subject enrollment and drug supply management in any clinical trial.
eCaseLink CTMS
eCaseLink, DSG’s web based Clinical Trial Management System (CTMS), is a project management application that helps you to capture and share a wide variety of clinical trial project status information across multiple studies. eClinDirect gives you unparalleled control over your clinical trial study.
eCaseLink Safety
The eCaseLink Safety system enables medical monitors to electronically record the SAE form information received from a site. Enter data into forms manually, as well as prefill certain fields mapped from the eCaseLink EDC system. Key events, dates and status are all easily tracked. The Drug Safety system alerts the medical monitor to differences between the safety data entry form and the data entered into eCRFs within the eCaseLink EDC system.
eCaseLink.Me / ePRO
eCaseLink.Me provides a flexible approach to patient-reported data capture that can be used alone or in combination with eCaseLink EDC software for reporting and data analysis. Designed with the patient in mind, eCaseLink.Me allows patients to personalize and change the appearance of the application to better suit preferences. It works on any browser or web-enabled device.