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
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.
Data-driven and expert-led assessment of protocol viability, site selection, and recruitment planning to minimize trial risk and accelerate initiation.
Automation and expert support for regulatory compliance, clinical trial registry reporting, and disclosure workflows.
Optimizes strategy, protocol design, and portfolio management through analytics, domain expertise, and real-world data.
Digital platforms and campaigns to educate, identify, and enroll participants and healthcare providers using real-world and network data.
Regulatory document preparation and support for clinical trial registration, results disclosure, and compliance with summary requirements.
Design and deployment of APIs, analytic platforms, and dashboards for integrated data access, visualization, and workflow automation.
Regenerative Medicine
Digital Health Technologies
Show More (5)Drugs
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
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.