The fastest and most accepted EDC solution for clinical trials is eCaseLink.

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8 out of 10 emerging biotechs choose dsg eClinical solutions

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DSG Solutions

We provide eClinical software and services to the life sciences industry.

DSG’s comprehensive and innovative suite of software provides unparalleled ease and flexibility for clinical trial success.

DSG’s data and project management services allows you to enjoy end-to-end support for critical milestones of your clinical trial.

DSG employs eSource and Risk Based Monitoring best practices into its eClinical suite, ensuring you are one step ahead for managing your clinical study.

DSG News & Events


BioPharma Asia 2018
  • 54th DIA Global Annual Meeting and Conference
  • Visit DSG at Island:#1770
  • Boston Convention and Exhibition Center
  • Boston, MA.
Enhancing the EDC experience with eCaseLink 10 from DSG
  • Boston, June 25, 2018

DSG, Inc. an industry leader in eClinical software and services to the life science industry, today announced that it will be releasing the newest version of their flagship eCaseLink™ EDC at the heart of their unified eClinical suite of products: eCaseLink10. This latest offering from DSG will be highlighted at the 54th DIA Global Annual Meeting and Conference, June 24-28 in Boston, MA at the Boston Convention Center.

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25 years of EDC eClinical solutions

About DSG

DSG, Inc. is a leading global eClinical provider with a fully unified suite of innovative technology solutions and data management services for the global clinical research community. DSG's eClinical software platform provides competitive advantage that is cost-effective with on-time project delivery. DSG solutions have been used in thousands of clinical trials around the globe with our award-winning eCaseLink™ platform and eCaseLink Designer for enterprise licensing. Founded in 1992, the company is proud to be recognized as the first provider of a fully integrated EDC and IRT Randomization and Trial Supply Management system with the SCDM Data Driven Innovation Award.

  • Studies up and running in less than two weeks
  • Industry leading technical support
  • Affordable and flexible pricing
  • Successful FDA submissions

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