Large Biopharma
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
Unify the latest digital technologies, new data sources, and advanced analytics, to realize your next breakthrough and propel your growth.
Adapt to anything
Respond to changing needs or new opportunities. Adapt to new challenges, integrate new technologies, and meet patient expectations.
Build for the future
Stay ahead of new disruptions, trends, and innovations. Invest in the technology that meets today’s opportunities and tomorrow’s transformation.
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.
Participants
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.
The Medidata Platform
The Medidata Platform connects patients, sites, sponsors, and partners in a secure and scalable cloud environment to support your business.
Manage your study from start to finish with one unified platform.
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
Global Pharma Bridges the Gap Between Data Management and Pharmacovigilance
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.
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.
Resources
Building Successful Diversity Initiatives in Clinical Trials through Stakeholder Engagement
Clinical trials continue to lack sufficient diversity, perpetuating inequitable access to novel therapeutics. Despite incremental progress over the past few decades, patient participation is still not aligned with the heterogeneity of intended treatment populations.
6 Data Linkage Use Cases to Future-Proof Your Clinical Trials
Accessing compelling and relevant evidence is crucial to drug development, safety monitoring, and improved patient outcomes. However, gaps between clinical trial data (CTD) and real world data (RWD) make it difficult to fully understand what happens to patients outside of a clinical trial. These gaps hinder evidence generation and result in missed insights.
Improve Data Review Efficiency with Powerful Patient Data Surveillance
Ensuring data quality and patient safety oversight during clinical trials requires multiple operational team members to aggregate, interrogate, and query data across EDC and other sources.