Central Laboratories White Papers & Articles
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The Transformation Of Regulatory Processes Through AI, ML, NLP, And RPAs
4/7/2025
Explore the rapidly evolving landscape of regulatory processes as they undergo a profound digital transformation, highlighting how emerging technologies are reshaping traditional regulatory frameworks.
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Key AI Trial Insights From Regulators And Consultants
4/4/2025
AI’s transformative impact promises more efficient, cost-effective, and successful clinical trials across the pharmaceutical landscape.
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Implementing An ERP System: 5 Key Steps To A Successful Rollout
4/3/2025
Key success factors to implementing an ERP system include assembling a competent project team with leadership support, phased implementation to align with regulatory compliance, and careful data migration to ensure system reliability.
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Feasibility/Site Selection Process Ripe For Improvement
4/1/2025
One key to a more effective feasibility process is more transparent communications and collaboration between sponsors, CROs, and sites. Sponsors must provide clear information to each site to enable a more accurate recruitment assessment, and sites must properly digest the information to give an accurate projection. But how?
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The Future Of Pharmacovigilance: Integrating AI With Drug Safety Systems
4/1/2025
The use of AI in pharmacovigilance can enhance processes such as data analysis, signal detection, and case management by increasing efficiency, accuracy, and the ability to manage large datasets.
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The New Era Of Medical Monitoring
3/28/2025
Examine the transformative landscape of medical monitoring in clinical trials with an emphasis on the shift from conventional retrospective reviews to a proactive, risk-based methodology.
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2025 Trends In Patient Recruitment: From Disruption To Precision
3/27/2025
Explore the four macro trends reshaping the recruitment space in 2025—each grounded in emerging data, technology, and behavior shifts.
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A Data-Driven Approach To Clinical Trial Site Selection
3/24/2025
By incorporating data-driven site selection and verification, sponsors can optimize resource allocation, enhance protocol compliance, and improve overall trial integrity.
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Harnessing RWE For Effective External Control Arms In Clinical Trials
3/24/2025
Real-world evidence (RWE) is transforming clinical trials by enabling the use of external control arms (ECAs), which serve as an alternative to traditional randomized control groups.
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Advancing Neuroscience Research With Data-Driven Innovations And AI
3/24/2025
Learn how to employ data-driven insights, artificial intelligence, and decentralized clinical trials to accelerate drug development and address the intricate challenges of neuroscience research.