Citeline


Citeline offers data, analytics, and digital solutions to support clinical trials, drug development, and regulatory compliance. Their capabilities include AI-powered clinical planning, site selection, patient engagement, real-world data integration, regulatory reporting automation, and in-depth industry analysis for the global life sciences sector.

Citeline

Citeline


What We Do

Platform aggregating global clinical trial, investigator, site, and drug pipeline intelligence for planning and competitive analysis.

Software platform for automating regulatory disclosure, trial registry submissions, compliance tracking, and risk mitigation.

Digital platform for identifying, engaging, and enrolling participants using real-world data and eligibility matching.

Platform integrating consulting and analytics for clinical development and real-world evidence utilization.

Web-based solution for aggregating and distributing lay summaries of trial results to enhance understanding and regulatory transparency.

Aggregates clinical trial, investigator, and site data with analytics to inform clinical development and operational planning.


Regenerative Medicine

FDA Regulated Medical Devices


Key People

Disclosure Regulations Research Manager

Editor in Chief, Commercial Insights

VP of Global Transparency

Executive Director, News and Insights

Editor-in-Chief, APAC

Interim Editor-in-Chief, Pink Sheet

VP Custom Content


News & Updates

Enabled recruitment of pediatric, ultra-rare disease patients for a clinical trial with digital tools for prescreening eligibility.

Launched a comprehensive, tokenized dataset combining real-world data with clinical, regulatory, and commercial intelligence.

Supported participant enrollment for a large Phase III COVID-19 vaccine trial via integrated engagement solutions.

Explores the use of real-world data to improve recruitment in clinical trials.

Examines the influence of real-world data on clinical research strategy and planning.

Impact of the US government shutdown on clinical trial registration and compliance.

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