Our Story

Every clinical trial begins with a vision — to advance medicine and bring breakthrough therapies to life. Medigen Suite™ supports that vision as a compliance-ready eClinical platform, unifying clinical data, imaging workflows, trial operations, and patient engagement. From first patient in to regulatory submission, it ensures data integrity, smooth execution, and informed decisions across global clinical trials.

Built on Real Clinical Experience

Medigen Suite™ was developed in 2009 by experts in clinical research and healthcare technology. It draws on the operational expertise of Meditrial, a leading CRO known for guiding innovative medical device, drug-device, and pharmaceutical studies worldwide. By applying lessons from real-world trials, Medigen Suite tackles the complexity of modern clinical studies, replacing fragmented systems with a configurable, scalable and regulatory-ready platform. This connection ensures global study teams can run trials efficiently, maintain compliance, and deliver high-quality results.

As clinical trials grew more complex, Medigen Suite evolved into a fully connected ecosystem, combining Catchtrial EDC and Maptrial CTMS. It centralizes oversight, accelerates study startup and ensures regulatory-ready, scalable deployments.

Key features include:

  • Unified data management and analytics
  • Reusable templates and centralized workflows
  • Interoperability with EHR, lab, imaging, and safety systems
  • Secure clinical and imaging data capture, eConsent and decentralized trial tools
  • Regulatory-ready deployments with audit-ready dashboards and AI insights.

All modules are fully integrated, allowing data, workflows and oversight to flow seamlessly across the entire trial lifecycle.

Timeline of Medigen Suite™

Grounded in Meditrial’s clinical operations, the Medigen Suite evolved through sustained learning and innovation. This journey traces how experience shaped a modern eClinical platform supporting complex clinical research worldwide.

You Run Trials.
Let Us do the Rest.

Find out how the Medigen Suite can fully support your clinical trials, connecting every step of the process and accelerating your path to market.

Solution Spotlight

Catchtrial EDC simplifies capture of clinical and imaging data, ePRO/eDiary, eConsent, and automated validation. Maptrial CTMS provides centralized oversight, monitoring, site tracking, and audit-ready dashboards. Together, they form a connected Medigen Suite ecosystem for end-to-end clinical trial execution — so your team can focus on innovation while Medigen handles the complexity.