Featured Articles
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Disclosure Management System: Build Or Buy?
6/19/2025
Clinical trial disclosure regulations are tightening worldwide. In order to maintain compliance, sponsors must determine whether to build an internal disclosure management system or buy a solution.
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New Data Sources Can Help Pharma Meet Challenges
6/19/2025
Claire Riches, Citeline VP of Clinical Solutions discussed the changing pharma landscape and data options, such as RWD, RWE, and AI at Citeline Elevate Spring 2025.
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Completed Clinical Trials Continued To Climb In 2024
6/19/2025
Data collected in this report reflects a shift toward sustained growth, reflecting rapid advancement in therapeutic areas such as oncology, autoimmune/inflammation, and central nervous system studies.
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Data Key In Addressing Patient Recruitment Challenges
6/19/2025
Explore how a Phase II trial for extensive-stage and previously treated small cell lung cancer overcame recruitment challenges with a data-driven solution designed to surface protocol-matched patients.
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Zeroing In On The Right Patients With RWD & Proprietary Data
4/28/2025
Complex I/E criteria? Seeking broad demographic representation? Don’t know where to find eligible patients? No problem! See how comprehensive data and a connected ecosystem combine to revamp recruitment.
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The Future Of Patient Recruitment: Leveraging RWD For Precision
4/25/2025
To combat the costly challenges of patient recruitment and keep trials on track, sponsors can leverage real-world data.
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Unlocking The Potential of RWD In Clinical Trial Recruitment
4/25/2025
Explore how real-world data (RWD) is transforming recruitment strategies and leveraging technologies such as AI and machine learning.
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Overcoming Complex Patient Recruitment Challenges With Data
4/15/2025
Overcome roadblocks to recruiting patients for rare disease clinical trials with RWD and RWE, including lack of diagnosis and stringent I/E criteria, geographic dispersion, and high dropout rates.
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Global Trial Disclosure Landscape Grows Increasingly Complex
4/15/2025
The industry is witnessing a global trend toward increased transparency and more stringent enforcement of clinical trial reporting requirements. However mechanisms and penalties differ significantly across regions and countries.
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Faster Trial Planning and Site Selection
4/15/2025
Address the challenges of identifying the most suitable trial sites and investigators while optimizing feasibility planning, reducing screen failure rates, and improving patient retention.