Medidata Unveils Next-Generation Patient Consent Innovations, Designed in Partnership with Clinicians and Patient Advocates
Medidata Consent, a key part of the , expedites study start-up, reduces configuration complexity, and improves patient enrollment
NEW YORK, Oct. 30, 2025 (GLOBE NEWSWIRE) -- , a Dassault Systèmes brand and leading provider of clinical trial solutions to the life sciences industry, today announced notable advances to , its industry-proven electronic informed consent technology. Delivered through the , this modern solution reimagines patient consent in clinical trials – focusing on adaptability, usability, and global compliance to remove adoption barriers and amplify subject recruitment from the very first patient interaction.
"At Medidata, we believe true innovation comes from listening to our customers and the patients they serve. Our updated Consent solution is a direct result of feedback from sites and sponsors who needed a simpler, more flexible way to manage the consent process,” said Matt Noble, senior vice president, Patient Experience, Medidata. “We've redesigned Consent to be more intuitive, empowering both patients and researchers while streamlining a critical step in the clinical trial journey."
This solution optimizes clinical trial enrollment by simplifying study designs, elevating the user experience for sites and patients, and offering sponsors real-time visibility into the consent process. Key features include:
- Accelerates Study Builds with AI-Assisted Setup: An AI-automated workflow significantly shortens study configuration by mapping documents for e-signatures, reducing manual effort by up to 75%.
- Delivers an Intuitive Experience: Patients benefit from a simplified and interactive interface, while site staff work within a familiar, unified environment that reduces friction and improves adoption. These frameworks are informed by direct collaboration with the and .
- Seamlessly Integrates with the : Native integration with and the broader Medidata ecosystem eliminates duplicative data entry and manual reconciliation. Unlike bolt-on tools, Consent is part of a truly unified platform, which avoids data silos across Medidata systems.
Future enhancements will expand Consent’s remote capabilities, allowing participants to register from anywhere and engage with personalized educational content, improving comprehension of the study process and fostering more meaningful conversations with investigators.
To learn more about Medidata Consent, please visit .
About Medidata
Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 36,000 trials and 11 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata’s seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at . Listen to our latest podcast, , and follow us at @Medidata.
About Dassault Systèmes
Dassault Systèmes is a catalyst for human progress. Since 1981, the company has pioneered virtual worlds to improve real life for consumers, patients and citizens. With Dassault Systèmes’ 3DEXPERIENCE platform, 370,000 customers of all sizes, in all industries, can collaborate, imagine and create sustainable innovations that drive meaningful impact. For more information, visit: .
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