New York – October 7, 2021 -- Medidata, a Dassault Systèmes company, today announced the launch of Medidata Link at NEXT Global 2021. Medidata Link is the only centralized solution to connect patient-level clinical trial data and real-world data (RWD) – powered by and fully integrated with the Medidata Unified Platform – providing any clinical trial run on Medidata Rave EDC (electronic data capture) the option to conduct data linkage.
“Medidata Link provides the opportunity to enhance evidence generation activities, including needs that were not originally anticipated, which allows sponsors to collect trial data and connect it to patients’ RWD,” said Sastry Chilukuri, co-CEO of Medidata. “This transformational capability bridges evidence gaps, and helps create the insights necessary to save time and bring more confidence in clinical decision making.”
Medidata Link enables customers to generate a “token” to connect the patient’s clinical data in the Medidata Unified Platform to the industry’s broadest RWD ecosystem in a secure, compliant, and scalable manner. Medidata facilitates the de-identification process by providing a user-friendly collection process for Personally Identifiable Information (PII) through site-facing capabilities and the myMedidata patient portal. This creates a seamless integration with the rest of the clinical trial workflow and is agnostic of consent methods. The solution protects sponsors from the risks of directly holding PII, while streamlining third-party data privacy certifications so that only certified data is transferred to sponsors. Medidata is partnering with HealthVerity and Datavant to establish pre-built integrations to enable this de-identification and linkage to a broad RWD ecosystem.
Medidata Link helps sponsors, trial sites, and patients to:
Medidata Link offers a significant opportunity to better understand a patient population and therapeutic outcomes before, during, and after the trial. By connecting patients participating in a trial to RWD, drug developers can save years by not having to wait until the trial concludes to start generating real-world evidence (RWE) that can inform medical and future pipeline decisions. Unrivaled in analytics, clinical and commercial expertise, Medidata allows sponsors and CROs to generate the best evidence and insights from their connected data.
Medidata is a wholly owned subsidiary of Dassault Systèmes, which with its 3DEXPERIENCE platform is positioned to lead the digital transformation of life sciences in the age of personalized medicine with the first end-to-end scientific and business platform, from research to commercialization.
Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 1,700+ customers and partners access the world's most trusted platform for clinical development, commercial, and real-world data. Medidata, a Dassault Systèmes company (Euronext Paris: FR0014003TT8, DSY.PA), is headquartered in New York City and has offices around the world to meet the needs of its customers. Discover more at www.medidata.com and follow us @Medidata,
Dassault Systèmes, the 3DEXPERIENCE Company, is a catalyst for human progress. We provide business and people with collaborative virtual environments to imagine sustainable innovations. By creating 'virtual twin experiences’ of the real world with our 3DEXPERIENCE platform and applications, our customers push the boundaries of innovation, learning and production.
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