Large Biopharma: Clinical Trial Solutions
Adapt, innovate, and scale for the future
Global pharma and biopharma companies like yours partner with Medidata to accelerate timelines, streamline processes, drive efficiencies and stay at the forefront of the industry.
Why Global Industry Leaders Trust Medidata
You and your team are under pressure to continually innovate, adapt to disruptions, focus on patient centricity, detect risks earlier, and scale at an unprecedented pace to get therapies to market faster.
With 20+ years of industry leadership, Medidata empowers 19 of the top 20 biopharma companies to meet the demands and opportunities of every trial environment.
Innovate with proven technology
Adapt to anything
Build for the future
Experience Matters
With over 2 decades of worldwide collaboration with customers, patients, and partners, Medidata delivers smarter treatments and healthier people.
Clinical Trials
Thousands of studies in 140+ countries have been conducted on the Medidata platform.
Patients
Over 10 million patients across Medidata trials have impacted clinical research and touched countless lives.
of the top 20 pharma companies
95% of the top 20 pharmaceutical companies use Medidata technology.
Of FDA-approved Drugs
More than 7 out of 10 novel drugs approved by the FDA in 2022 were developed on Medidata software.
Your Technology Roadmap through the
Clinical Trial Process
Clinical trials are inherently complex and challenging to navigate and the right technology can help. Sponsors struggle with deciding which technology is right for their study requirements.
This clinical trial roadmap illustrates the technologies that add the most value at each step of a trial. No matter where you are in your trial process, design and planning, start-up, collecting and managing patient data, or closing out, step through the roadmap for guidance to bring your trial to a successful conclusion.
A Few of Our Partners & Customers
Biotech Delivers a Superior Patient and Site Experience with the Medidata PlatformSite Count
See how Rezolute leveraged the Medidata Platform to create a superior patient and site experience in a pediatric rare disease trial.
A Mid-sized Sponsor Increased its Potential Site List for a Rare Disease Clinical Trial by 50% with Medidata AI Intelligent Trials
As they embarked on an upcoming rare disease clinical trial, a mid-sized biopharmaceutical company was struggling with patient recruitment and site selection. The company needed to identify sites with the greatest access to patients and highest enrollment performance but did not have deep enough data to make confident decisions. See how Medidata AI Intelligent Trials helped solve the site challenge.
Medidata’s Full-Service Site Payment Solution: Mid-sized Sponsor Manages Study Finances across Hundreds of SitesSite Count
A sponsor is on a mission to conquer cancer with data, empowering patients and providers to act decisively in fighting the disease. Shortly after the sponsor became publicly traded, the company planned to sponsor its first large clinical trial. Recognizing that the financial management of the study would be as critical to the trial’s success as data management, the sponsor turned to Medidata’s Rave Site Payments solution to track and manage timely payments to research sites, triggered by entries in Medidata’s Rave EDC (Electronic Data Capture) solution.
A Top 10 Pharma Company Doubles High-Performing Site Count
A top 10 biopharmaceutical company was looking to gain agility and confidence in their trial planning, site selection, and enrollment decisions in a priority indication. The sponsor wanted to expand their site list and gain a deeper understanding of how existing sites in their database performed.
Global Pharma Bridges the Gap Between Data Management and Pharmacovigilance Site Count
A global life sciences organization engaged in an initiative to significantly improve clinical productivity. This industry leader typically has hundreds of new treatments in development at a time in all trial phases. The capture, triage and reporting of serious adverse events (SAEs) by local and central pharmacovigilance (PV) groups is a critical process that runs concurrently with data management.
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