Central Laboratories White Papers & Articles

  1. Where PRO Strategy Goes Wrong 5/27/2026

    PRO and COA strategy is now central to trial success. Organizations that capture meaningful patient experience data will gain stronger evidence and a regulatory advantage.

  2. Is The Industry Ready To Trust LLMs With Chart Review? 5/27/2026

    See how LLM-powered extraction transforms unstructured medical records into compliant, audit-ready clinical data with machine-scale speed, human oversight, and regulatory-grade accuracy.

  3. Artificial Intelligence, Virtual Participants, and the Evolving FDA Regulatory Landscape 5/27/2026

    Understanding emerging requirements around transparency, risk, and governance is essential for responsibly advancing AI-driven innovation in regulated environments.

  4. The Regulatory Governance Gap In Clinical Trial AI 5/21/2026

    Regulators are no longer questioning whether AI belongs in clinical trials; however, they’re demanding a governed infrastructure that makes every AI-driven decision auditable and defensible.

  5. Capture Was Step One. Execution Is Step Two. 5/21/2026

    Electronic data capture transformed clinical trials, but advancing a study depends on decision workflows that interpret data, coordinate teams, and determine meaningful next actions.

  6. De-Risk Trials For Accelerated Approval And Pipeline Optimization 5/20/2026

    This e-book explores how AI-powered Historical Clinical Trial Data (HCTD) is reshaping modern trial design for oncology and rare disease research.

  7. Rethinking How We Forecast Clinical Trial Timelines 5/12/2026

    Machine learning is transforming clinical trial reporting by replacing static enrollment forecasts with dynamic, real-time milestone projections that improve predictability and oversight.

  8. State of Materiovigilance: Gaps, Technology & Outsourcing 5/12/2026

    Explore how pharma and biotech companies are using AI, outsourcing, and new technologies to strengthen materiovigilance for complex drug-device products.

  9. Reducing Inventory Errors In Clinical Trials 5/8/2026

    Can a digital double-check save your trial from data errors? How does verifying shipments at receipt slash inventory mistakes? Learn to protect protocol integrity and patient safety.

  10. Transparency In Action: The Key To Trust And Efficiency 5/8/2026

    Trust is the backbone of clinical research. Learn how you can utilize transparency and data integrity to protect participants, meet regulatory standards, and drive medical innovation.