For over 24 years, DSG has implemented Standard Operating Procedures that get your clinical trial study up-and-running when you need it. Our experienced staff of Project Managers, Trainers, and Quality Assurance Professionals will make sure that your study is deployed in a timely, efficient manner that accomodates your deadlines.
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Shortest setup time from Final Protocol to Clinical Trial Study Launch
Set-up time for the data entry screens and database is minimal. Using its proven ProBuild Tool, DSG links data-entry fields to the corresponding database fields through a point-and-click interface. This makes it easy to create and edit messages and to warn of data-entry errors at the field level. There is no need to design specific EDC screens or write code, which delays study roll-out. Through ProBuild, data-entry screens for visits can be posted and deployed to sites as soon as they are finalized. Mid-study changes are completed with the same ease and quick turnaround as start-up using this same process, eliminating delays and additional costs that are often associated with other EDC systems. Testing and posting of new forms are completed within hours of receiving change requests, without disruption to the sites and keeping costs at a minimum.
Experienced Project Management Services
Exceptional customer service is the cornerstone of DSG's success. With over 20 years experience in deploying clinical trials, our Project Management methods are unsurpassed in the industry. All of our (PMs) Project Managers are fully trained to guide the eCRF design, edit specification approval, training and data export programming; while keeping you informed and involved every step of the way. Sponsors benefit from having one Senior Project Manager, one Associate Project Manager and one Account Manager dedicated to their study. Our project managers are trained in the life science industry to provide the expertise where you need it.
On-Demand Data Export Programming
DSG will perform the initial on-demand data export programming to ensure that your clinical trial data is ready for analysis at any point in the study. That means any user with designated data management privileges is able to generate real-time on-demand data sets during a study with the click of a button. You can get instant on-demand data exports formatted automatically and converted to a zipped file. Perform real-time on-demand data analysis in an easy-to-use point-and-click interface, anytime, anywhere.