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.
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.
FDA outlines updated requirements for expanded access to investigational drugs and trial result transparency.
Discussion of regulatory and best practice strategies for producing patient-accessible trial result summaries.
Annual C+D Awards recognizing achievements and innovation in the UK community pharmacy sector.
17th annual C+D Awards event celebrating achievements in community pharmacy in London.
Webinar on registry harmonization and transparency improvements in clinical trials.
Webinar addressing regulatory practices for plain language summaries in clinical trial result communications.
Visual summary of recent trends in China's pharmaceutical sector, including innovation and global partnerships.