Central Laboratories Solutions

  1. Driving Success In Dermatology Drug Development

    Our dedicated teams are led by in-house, board-certified dermatologists who have decades of experience conducting early and late phase studies. Download the available brochure to learn more.

  2. Aligning Site And Patient Needs For Clinical Trial Success 4/17/2025

    Redefine clinical trial execution by aligning site and patient needs through a unified, intelligent platform.

  3. TA Scan: Clinical Intelligence Platform 4/20/2023

    Start making data-driven decisions for your clinical trial workflows by utilizing this platform to analyze, measure, and rank trial and site data, including KOL and PI experience and involvement.

  4. Fast-Track Your Move To Oracle Argus 4/26/2024

    rapidLIVE for Oracle Argus is tailored to meet the specific needs of safety and clinical teams across various organizations, including biopharmaceutical, medtech firms, and CROs of all sizes.

  5. Medidata Research Alliance: Partnerships For Medical Progress 2/15/2024

    Learn about the strategic partnerships, collaborative models, and impactful work that define the Medidata Research Alliance and drive advancements in medical knowledge and patient care.

  6. Feasibility As A Service From Consulting & Analytics 11/26/2024

    Citeline’s Feasibility as a Service (FaaS) leverages data-driven insights to enhance clinical trial success by providing comprehensive feasibility assessments.

  7. Clinical Data Studio: Unlock The True Power Of Clinical Trial Data 4/15/2024

    Unlock the full potential of clinical research data with Medidata Clinical Data Studio. Simplify processes, accelerate timelines, and enhance data quality with AI-powered offerings.

  8. Clinical Pharmacokinetics And Pharmacometrics 4/11/2025

    Learn about a sophisticated suite of pharmacokinetic (PK) and pharmacometric services designed to accelerate and optimize early-phase drug development.

  9. Rave TSDV - Improve CRA Efficiency And Reduce Site Burden 12/20/2023

    Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.

  10. Risk-Based Monitoring 9/26/2023

    Program, country, and study managers, CRAs, clinical monitors, trial managers, clinical data managers, CROs, and others need informatics solutions that help them focus on sites in greatest need, based on risk.