Central Laboratories Solutions

  1. Real World Data 6/27/2023

    Accelerate patient recruitment and drug development with real world data (RWD).

  2. Bring Your EDC Study In-House 6/17/2024

    The EDC module with Signant SmartSignals® Unified Platform, trusted in over 3,000 trials, allows in-house teams to design studies easily with minimal training and no coding skills needed.

  3. Financial Scenario Planning 4/12/2024

    Discover how Financial Scenario Planning empowers clinical trial budgeting with agile modeling, compliance, risk mitigation, and transparent insights for informed decision-making.

  4. A New Blueprint For Transforming Feasibility And Recruitment 10/20/2025

    Clinical trials often fail due to poor feasibility planning. A new AI-powered approach bridges protocol design with real-world patient access to improve enrollment success.

  5. Comprehensive Data And Analytics For Cell, Gene, And RNA-Based Therapies 10/19/2022

    Stay on top of changes in the ever-evolving world of cell and gene therapies and more. Our in-house subject matter experts comb through the data weekly to ensure we provide you with the most current and comprehensive information important to this market.

  6. The Path To Proof, Reimagined 5/15/2024

    By combining technology with clinical and operational expertise, Signant Health prioritizes the clinical research stakeholder experience, making it more intuitive, while ensuring the data journey is direct.

  7. 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.

  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. 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.

  10. Rave TSDV - Improve CRA Efficiency And Reduce Site Burden 1/5/2026

    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.