Services

  Click to view enlarged screenshot

  Click to view enlarged screenshot

Implementation & Project Management

When we say “Trials at the Speed of Technology,”
we mean it.

For over 6 years, DSG has implemented Standard Operating Procedures that get your 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.

• Shortest Time from Final Protocol to 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
  Exceptional customer service is the cornerstone of DSG's success. With over 20 years deploying clinical trials, our Project Management experience is unsurpassed in the industry. All of our PMs 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.
• SAS and data export programming
  DSG will perform the initial data export and SAS 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 SAS data sets during a study with the click of a button. You can get instant data exports in SAS format in an automatically zipped file. Perform real-time SAS data analysis in an easy-to-use point-and-click interface, anytime, anywhere.