Intelligent Trials

Increase confidence in decision making across a clinical trial’s life cycle – from study planning through execution – to bring treatments to patients faster. With our turnkey solution that provides unmatched site-level granularity and actionable real-time industry-wide insights, you can reduce trial timelines, prevent enrollment delays, enroll more diverse patients, and ensure success of your clinical program.

Benefits of Clinical Trial Analytics

Identify study footprint

Determine realistic timelines and study footprint by assessing enrollment rates of industry trials and selecting which countries and number of sites would be needed to meet timeline goals.

Learn more about Intelligent Trials Study Feasibility.

Select high-performing sites

Improve site selection to meet enrollment timelines leveraging industry-wide, real-time and historical enrollment performance and predictive analytics.

Learn more about Intelligent Trials Study Feasibility.

Enroll more diverse patients

Establish clinical trial diversity goals and enhance site selection to choose sites that can accelerate your trial and are more likely to enroll diverse patients, based on indication-specific cross-industry data.

Learn more about the Intelligent Trials Study Feasibility Diversity Module.

Accelerate enrollment

Identify opportunities to improve operational performance and accelerate enrollment
by comparing your trial to the performance of industry trials and forecasting enrollment.

Learn more about Intelligent Trials Performance Analytics.

Key Features

01 Industry’s largest performance dataset

Industry’s largest performance dataset

Cross-pharma and CRO dataset that spans over 30k trials and 9M patients, adding unique value to even our largest customers.

02 Unmatched site-level granularity

Unmatched site-level granularity

Metrics span operational and diversity performance, enabling selection of sites that will accelerate the study and increase clinical trial diversity.

03 Actionable real-time insights

Actionable real-time insights

Unique insights leveraging data refreshed weekly from ~8k active studies, allowing customers to calibrate performance and take action within a competitive landscape.

04 Turnkey with white-glove support

Turnkey with white-glove support

Off the shelf SaaS solution and API access combined with white glove service support customers in making confident decisions.

Learn More

Featured Whitepapers and Reports

The State of Black Participation in Clinical Trials

In our new research report, we set forth to assess the current state of racial diversity beyond the FDA Snapshot, using Medidata’s industry-leading clinical trial data repository.

Featured Case Studies

Medidata AI Supports PPD’s $60M Study Award in Rare Oncology Indication

With Medidata’s broad industry performance data and Study Feasibility solution, PPD was enabled to reduce the projected clinical trial timeline and be awarded a key $60M study in a rare oncology indication.

Featured Podcasts and Webinars

ASCO Education: Racial Disparities in Clinical Trial Participation

Learn about the state of clinical trial diversity in clinical trials and what clinicians and trial sponsors can do to improve participant diversity.

Featured Blogs

How Pharmaceutical Companies Can Achieve Success Amidst Regulatory Focus

As new rules go into effect, learn about the top things pharmaceutical companies should consider to increase diversity in their clinical trial planning and execution, including enhancing site selection.