Central Laboratories White Papers & Articles

1. CRF Validation Best Practices: Building Reliable Clinical Trial Databases 11/5/2026

   CRF validation improves data quality and efficiency. Early planning, clear edit checks, and balance reduce rework, ease site burden, and enable more reliable, streamlined study execution.

2. Why More Sponsors Are Taking Control Of Clinical Trial Study Builds 11/5/2026

   Accelerate study startup and reduce rework by building studies directly in EDC. Discover a more flexible, efficient approach to managing clinical trials and data quality.

3. Improving Transparency And Credibility Of Real-World Evidence: The HARPER Template 11/2/2026

   HARPER brings consistency to real-world evidence studies, improving transparency and reproducibility while supporting clearer evaluation of methods and findings.

4. Omics-Driven Immune Challenge Design: What Early Human Data Tells Us 10/31/2026

   Transcriptomic and proteomic profiling of controlled human immune challenges shows which pathways, compartments, and time windows a model engages, helping match challenge choice to a drug's mechanism.

5. Beyond Automation: Transforming Clinical Trial Delivery Through Structured Information 10/23/2026

   Study build delays stem less from slow tasks than from protocol intent being reinterpreted at every handoff. Treating the protocol as structured, reusable information changes where AI and expertise belong.

6. Beyond Traditional CTMS And eTMF 10/21/2026

   Trial data scattered across spreadsheets, emails, and siloed systems slows teams down. Learn how connecting it gives one clear view that catches risks early and keeps studies inspection-ready.

7. The PMCF Decision Guide 10/14/2026

   Proposed EU reforms may remove standalone PMCF reporting, yet the duty to proactively collect clinical data remains. Method selection, notified body defense, and data-capture cost determine what comes next.

8. Reimagine Quality: Responding To EOL Deadlines 10/14/2026

   Delay, migrate, or reimagine? Learn how rethinking quality operations around AI can triple team productivity and keep you inspection-ready for the next decade.

9. Everything Clinical Trial Leaders Need To Know About AI Agents 10/13/2026

   A practical guide to what agentic AI actually means for clinical trials, from ontologies and human-in-the-loop governance to continuous validation and the build-versus-buy decision.

10. How Clinical Trials Are Moving From Digitized To Agentified 10/13/2026

    See how generative and agentic AI can streamline clinical trials, with independent analysis modeling up to $21M in value and 82x ROI for agent-enabled monitoring.