Innovative Solutions, Trusted Results
Medidata’s industry-leading clinical trials platform empowers CROs to navigate trial complexities with ease. Designed for user-friendliness and enhanced collaboration, we combine cutting-edge solutions with unparalleled partnership support to deliver seamless results for a better patient and user experience.
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Why CROs Choose and Trust Medidata
Introducing the Medidata Experiences, platform-enabled experiences built to manage complexity, digital solutions to streamline clinical trial processes, cut costs, speed up therapy evolution, and ultimately save patients’ lives.
Patient Experience
- Simplify patient participation
- Gain longitudinal engagement throughout a patient’s life cycle
- End-to-end patient-centric solutions break the transactional nature of patient engagement
Data Experience
- Simpler and faster data acquisition
- Automated data integration and transformation
- Accelerated actionable insights
- The solutions that Caidya has completed accreditations for are mainly attributable to the Data Experience: Rave EDC, Rave Coder, RTSM, Rave Coder, Site Cloud: End of Study, Clinical Data Studio (enabled)
Study Experience
- Accelerate clinical trial design, planning, and management
- Allows for better decisions with better data. Powered by AI and advanced analytics to seamlessly connect workflows, data, and teams
CRO Partners
including 9 out of the top 10 CROs, 134 for 5+ and 212 for 10+ years
Clinical Trials
including 2,000+ rare disease studies and 90% of oncology approvals in 2022
Patients
achieving >95% of patient compliance when using our tools
of FDA-approved drugs
developed on Medidata software in 2022
Learn About Our Partners
Whether our CRO Partners aim to fast-track study initiation, optimize trial outsourcing, enhance monitoring intelligence, or elevate the operational efficiency of their clinical trials, they trust Medidata to guide them every step of the way.
Success Stories from CROs
Choosing the Medidata Platform- The Common Denominator Amongst Sites
“Our CMO, our CEO, and I set out to ask sites what solutions they were accustomed to and what solutions they were comfortable with… The prevailing theme was they’ve used Rave EDC. And so, that became an anchor for us as we thought abouth whether or not to go the point solution route. After our due diligence and assessment of the different types of technologies we could step into, we decided to go with the [Medidata] Platform.”
-Keya Watkins, SVP, Clinical Development Operations for Catalyst Clinical Research
Medidata Clinical Data Studio AI- Endpoint Tracing and Predictive Capabilities
“Seeing the AI capability in Medidata Clinical Data Studio excited me, not only from a data management perspective… I also oversee our biometrics department. I’m looking [at] endpoint tracing- looking at endpoints, blinded or unblinded, using the AI to potentially project behavioral issues that could end up influencing your endpoint just by compliance measures- being able to have that AI component to tell you that, if this behavior continues at this event, you can have a lack of efficacy.”
-Michael Mendoza, Executive Director, eClinical Technology, Strategy & Biometrics for TFS HealthScience
Medidata AI: Adapting for People, Not the Other Way Around
“[Talking about AI in context to Medidata AI discussions:] In the past, people used to adapt and train to use the systems, but now the systems are adapting to people… using AI tools, using data visualizations, which are dynamically created on the spot.”
-Dilshat Djumanov, Director of Data Science for Richmond Pharmacology
Sponsors Request Medidata to Ensure Centralized Data Ingestion
“We’re getting big requests from sponsors to make sure that we’re using Medidata in a way that sees data get ingested onto that platform, creating a centralized location for sites and patients to work with.”
-Luke Gregory, Director, Clinical Systems for ICON
Integrating Complex, High Volumes of Data from Sensors and Multiple Data Sources
“Medidata integrates a lot of data sources and sensors in a streamlined way. Imaging is an important component in oncology that makes data collection and analysis easy. We navigate a maze between how much data we collect and submitting that to the FDA and other agencies. It is complex… integrating sensors, collecting more data, and having real evidence of what’s happening with our patients is key to he future of medicine and clinical trials.”
-Daniel Kowalski, Vice President, Biometrics for Kapadi
Leverage our Partner Program
Win. Innovate. Outperform.
Access exclusive tools and resources to drive growth and deliver on your sponsors’ needs for faster, more efficient, high-quality clinical trials.
Differentiate your business with the industry’s most comprehensive clinical trial technology across all phases, all therapeutic areas and levels of complexity. Leverage a world-class set of dedicated experts helping you to win more and outperform your competition.
Win. Innovate. Outperform.
Propel your commercial success, operational efficiency, and competitive edge.
Unlock your next-level market advantage with the technology, expertise, and support dedicated to you and your sponsors.