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.

Industries

clinical-trials

Nr. of Employees

large (251-1000)

Citeline

New York, New York, United States, North America


Products

Clinical trial data intelligence platform

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

Automated clinical trial disclosure and registry compliance platform

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

Patient recruitment and engagement digital platform

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

Consulting analytics platform for drug development

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

Plain language clinical trial summary platform

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


Services

Clinical trial intelligence and data aggregation services

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

Feasibility and site selection assessment for clinical trials

Data-driven and expert-led assessment of protocol viability, site selection, and recruitment planning to minimize trial risk and accelerate initiation.

Regulatory and clinical trial compliance management

Automation and expert support for regulatory compliance, clinical trial registry reporting, and disclosure workflows.

Consulting and analytics for clinical and drug development

Optimizes strategy, protocol design, and portfolio management through analytics, domain expertise, and real-world data.

Patient engagement, healthcare provider awareness, and recruitment solutions

Digital platforms and campaigns to educate, identify, and enroll participants and healthcare providers using real-world and network data.

Regulatory writing and disclosure submission services

Regulatory document preparation and support for clinical trial registration, results disclosure, and compliance with summary requirements.

View All Services

Expertise Areas

  • AI-powered clinical trial strategy
  • Protocol and feasibility optimization
  • Site and investigator selection
  • Clinical trial data analytics
  • Show More (6)

Key Technologies

  • Artificial intelligence for clinical trial design
  • Machine learning for investigator selection
  • EMR and real-world data integration
  • Synthetic data generation for modeling
  • Show More (6)

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