Central Laboratories White Papers & Articles
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Putting Trial Data Insights Into Action For Your Study
10/21/2025
Learn why sponsors should implement an integrated data monitoring plan and technology solution to ensure data integrity, meet evolving regulatory requirements, and improve trial outcomes.
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What We Learned At SCDM 2025 — And How To Act On It
10/20/2025
SCDM 2025 spotlighted six key shifts in clinical data management — from explainable AI to ICH-M11 — offering actionable strategies for teams embracing digital transformation.
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Designing More Precise Clinical Trials Using AI-Driven Analytics
10/20/2025
Clinical trials face staggering failure rates and inefficiencies. Discover how AI and real-world evidence streamline patient recruitment and trial design to help reshape the future of clinical research.
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Streamlining Patient Recruitment With AI–Driven Site Identification
10/20/2025
This study highlights the use of an RWD-driven, AI-enabled recruitment models as a transformative strategy for clinical development in hard-to-recruit populations.
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The EMR Interoperability Dream Vs. Clinical Research Reality
10/20/2025
Seamless Electronic Medical Record access promises accelerated trials and regulatory-grade evidence, but incomplete, unstructured data requires hybrid strategies using AI and human oversight to bridge gaps.
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Building Bioanalysis Infrastructure For Modern Drug Development
10/20/2025
Drug development accelerates with AI, decentralized trials, and adaptive protocols, but legacy CRO infrastructure lags. Platform-based systems enable speed, quality, automation, and continuous improvement.
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5 Outdated Practices Holding Back Modern Bioanalysis
10/20/2025
Bioanalysis must replace outdated paper, manual processes, and disjointed systems with integrated, automated platforms for continuous validation, efficiency, compliance, and to support complex modern therapies.
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Built Like A Tech Company: Why CROs Need A New Operating System
10/20/2025
See why building digital, automated infrastructure is essential, and better aligns CROs with today's speed, compliance, and innovation needs.
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Automated Evidence Generation For Regulatory-Grade RWD
10/20/2025
Global regulatory agencies increasingly adopt Real-World Evidence, demanding higher data quality and automated AI-driven platforms to meet evolving standards and improve drug development pathways.
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Recruitment Capabilities Delivering In Today's Trial Landscape
10/16/2025
Recruitment demands diverse capabilities — AI, data analytics, stakeholder engagement, operational excellence — to meet complex protocols and deliver high-quality patient enrollment outcomes.