THOMSON REUTERS CORTELLIS
FOR CLINICAL TRIALS INTELLIGENCE
Cortellis™ for Clinical Trials Intelligence includes global clinical trial protocols and outcomes for drugs, medical devices and biomarkers expertly uncovered and unified from a variety of data sources. It integrates with other key intelligence areas from Thomson Reuters including:
- drug pipeline
- deals
- patents
This intelligence provides unique insights that support a wide variety of strategic decision making. Additional delivery options include dynamic real-time visualizations, access to data via APIs, and integration with your existing knowledge platforms and workflow solutions.
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THOMSON REUTERS CORTELLIS
FOR COMPETITIVE INTELLIGENCE
Whether you're putting together a pipeline analysis, or developing a comprehensive competitive intelligence study,
Cortellis for Competitive Intelligence can get you to the critical information you need, faster.
Rapidly access the most current and accurate intelligence on:
- Drugs
- Patents
- Companies
- Deals
- Meetings
- Clinical Trials
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THOMSON REUTERS CORTELLIS
FOR REGULATORY INTELLIGENCE
Cortellis for Regulatory Intelligence gives you an innovative way to reach regulatory decisions faster. Powered by
IDRAC® — Thomson Reuters best-in-class regulatory intelligence — you can find the latest regulatory updates faster and easier than ever before. As a single, comprehensive source for global regulatory information,
Cortellis for Regulatory Intelligence provides all of the information you need to help you find your way and reach the right regulatory decisions, fast.
Covering 70 countries and more than 110,000 documents,
Cortellis for Regulatory Intelligence helps you keep up with the changing regulatory landscape via:
- Global Module — Compare regional requirements across multiple countries
- Regulatory Intelligence Reports — Track regulation changes, compare competitive products, and prepare for meetings and inspections
- Regulatory Summaries — Understand submission routes and local regulatory practices
- Reference Documents — Access up-to-date and historical regulatory documents
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