Central Laboratories White Papers & Articles

  1. RBQM: The Connective Tissue For Data Quality 1/13/2025

    RBQM integrates data-driven processes into clinical trials, ensuring enhanced quality and operational efficiency while emphasizing the synergy between QBD principles and robust data systems.

  2. Driving Enrollment Predictability In Clinical Trial Timelines 1/13/2025

    Missed enrollment targets cost millions—TA Scan’s benchmarking and simulation tools empower sponsors to forecast with confidence, optimize site strategy, and keep budgets on track.

  3. Five Steps To Preparing For The Product Management Service (PMS) Of EMA's SPOR Program 1/2/2025

    EMA's Product Management Service (PMS) database is crucial for IDMP compliance in the EU. Prepare for PMS requirements with this 5-step checklist that helps ensure smooth data migration and compliance.

  4. PIPA Conference Explores The Key Role Of PV 1/2/2025

    The PIPA 2024 conference emphasized the importance of pharmacovigilance across the pharmaceutical industry, from mergers and acquisitions to clinical trials and health authority inspections.

  5. Outlook For 2025: New Forces Driving Pragmatic Innovation 12/30/2024

    Clinical data trends are evolving rapidly to reduce trial complexity, improve patient experiences, and shorten development timelines.

  6. Understanding The Clinical Trial Process 12/30/2024

    This guide to clinical trials explores the regulatory approval, study startup, and trial processes essential for advancing medical innovation.

  7. Real Solutions To Simplify The Digital Data Flow 12/18/2024

    An efficient flow of complex data is critical for timely, informed decision-making during clinical trials. Explore four key strategies to simplify your digital data flow.

  8. 2025 Safety And Regulatory Compliance Trends And Predictions 12/16/2024

    Explore the rapidly evolving regulatory landscape that pharmaceutical and biotech industries face as they integrate AI and advanced technologies into safety, compliance, and lifecycle management.

  9. Artificial Intelligence Regulation 12/13/2024

    To make the best use of artificial intelligence (AI), drug sponsors need to understand where health authorities are drawing the lines.

  10. How To Differentiate With A Unified eClinical Solution 12/9/2024

    Clinical trials are increasingly complex for sites, sponsors, and CROs. In a recent webinar, experts Bill Byrom and Jan Breemans shared how a unified eClinical platform simplifies operations and enhances data quality.