The fastest and most accepted Clinical Trial Management Software is eCaseLink.

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8 out of 10 emerging biotechs choose dsg eClinical solutions

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Big Enough to Meet Your Needs, Small Enough to Care

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DSG Solutions

We provide electronic data capture (EDC) software, data management, and other clinical trial services for the life sciences industry.

DSG’s comprehensive and innovative suite of software provides unparalleled ease and flexibility for your 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 CTMS, eSource and Risk Based Monitoring best practices into its eClinical suite, ensuring you are one step ahead for managing your clinical study.

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Outsourcing in Clinical Trials – Southern California 2019

OCT – logo
Come join us for OCT 2019 in La Jolla, Southern California!
  • September 24th – 25th, 2019

The primary delegates for the OCT Medical Devices 2019 event are those with responsibility for clinical operations, outsourcing, procurement and alliances in biotech and pharmaceutical companies in Southern California. This will be a great opportunity to meet the DSG team and to experience our latest eClinical software and clinical data management solutions.

Schedule a Meeting Upcoming Events »
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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Years of Experience

Client Testimonials