Medidata Solutions
Provides a unified clinical trial platform and data services that combine AI, real-world data, and integrated clinical data capture to support study design, execution, and evidence generation across sponsors, CROs, and sites. Focus areas include AI-driven study design and protocol optimization, unified electronic data capture and imaging data management, real-world data analytics (including synthetic control arms), and tools for operational visibility and regulatory-ready data quality.
Industries
N/A
Nr. of Employees
small (1-50)
Patents
Products
Core lab‑agnostic imaging data management
A system for secure ingestion, de-identification, automated edit checks, routing, and real-time review of imaging data across sites, core labs, and sponsors.
Real-world data and synthetic control arm design service
Analytical services that construct synthetic/external control cohorts from historical trial data to support hybrid trial designs and regulatory engagement.
Patient-facing data capture and sensor integration
Solutions for eCOA, patient apps, and wearable sensor data capture that feed securely into central trial datasets.
Risk-based monitoring and targeted source document verification
Tools and operational services for TSDV and centralized monitoring to improve data quality and reduce manual review.
Core lab‑agnostic imaging data management
A system for secure ingestion, de-identification, automated edit checks, routing, and real-time review of imaging data across sites, core labs, and sponsors.
Real-world data and synthetic control arm design service
Analytical services that construct synthetic/external control cohorts from historical trial data to support hybrid trial designs and regulatory engagement.
Patient-facing data capture and sensor integration
Solutions for eCOA, patient apps, and wearable sensor data capture that feed securely into central trial datasets.
Risk-based monitoring and targeted source document verification
Tools and operational services for TSDV and centralized monitoring to improve data quality and reduce manual review.
Services
Cloud-based EDC and clinical data management connecting multiple data sources (eConsent, eCOA, imaging, RTSM, sensors) and providing centralized analytics and review.
Cloud-based EDC and clinical data management connecting multiple data sources (eConsent, eCOA, imaging, RTSM, sensors) and providing centralized analytics and review.
Expertise Areas
- Clinical trial management
- AI-driven trial design and protocol optimization
- Real-world evidence and synthetic control arms
- Imaging data management for clinical trials
Key Technologies
- Artificial intelligence / machine learning
- Real-world data analytics
- Synthetic control arm methodologies
- Electronic data capture (EDC)
News & Updates
Announcement of AI-focused presentations and demonstrations at a company conference highlighting AI companions and orchestrated intelligence for life sciences.
Partnership to deploy AI-driven study build technology to accelerate oncology studies.
Announcement of an integration enabling over 2,500 research sites to connect systems and accelerate trial operations.
Summary of company impact of AI across hundreds of clinical studies over ten years.
Recognition of an AI-based protocol optimization capability with an industry award.
Announcement of AI-focused presentations and demonstrations at a company conference highlighting AI companions and orchestrated intelligence for life sciences.
Partnership to deploy AI-driven study build technology to accelerate oncology studies.
Announcement of an integration enabling over 2,500 research sites to connect systems and accelerate trial operations.
Summary of company impact of AI across hundreds of clinical studies over ten years.
Recognition of an AI-based protocol optimization capability with an industry award.