Our extensive team of trial experts and analysts tracks over 30,000 information sources, delivering a unique combination of reliable data and unlimited personal research support.
Citeline covers every stage of drug development, featuring over 225,000 drug trials across 150 countries and more than 180 diseases.
Our PhD and MSc-level analysts conduct support research on your behalf at no additional cost, helping you to gain deeper competitive pharma business intelligence on specific trials within just 48 hours.
Citeline examines over 373,000 clinical trial investigators, assessing their ability as well as their expertise in specific pharmaceutical clinical trials, giving you access to the most extensive dataset of investigator expertise, experience and capacity.
Citeline has designed proprietary pharmaceutical clinical trial algorithms to help you better predict clinical trial timelines, from patient enrollment through study duration period and trial completion.
The full suite of Citeline pharmaceutical clinical trial products has been developed to allow easy cross-navigation, allowing you to move seamlessly from pipeline analysis and drug trial records to profiles of clinical trial investigators.
To review the impact of the US Food and Drug Administration's expedited approval pathway on drug development and regulatory review to date, check out a infographic created by our sister businesses Biomedtracker, Pink Sheet (FDA Performance Tracker),
The Citeline family of pharmaceutical clinical trial intelligence products.
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