Central Laboratories Products/Services

  1. Computer Systems Assurance And Validation 7/22/2025

    Computer System Validation to cover all your GMP, GLP, GCP, and QA/QC software applications. CompliancePath currently has 30+ active projects globally supporting clients in CSV/CSA compliance.

  2. Ergomed's Risk-Based Quality Management 2/6/2025

    Ergomed’s Meticulous Risk-Based Quality Management Approach

    As a pioneer in providing comprehensive support for your clinical research, Ergomed champions an innovative Risk-Based Quality Management (RBQM) approach. This forward-thinking strategy ensures the highest patient safety standards, regulatory compliance, and data reliability. Ergomed’s proactive approach to managing clinical trials tackles clinical research complexity head-on.

  3. Suvoda IRT 9/16/2025

    A centralized command center for patient randomization and drug supply management—built for today’s complex clinical trials.

  4. BIOGRID: The Most Effective Way To Graphically Represent Data-Driven Insights 9/28/2022

    Bioforum’s clinical research experts have developed an intuitive and easy-to-navigate analytics and visualization platform.
    BioGRID brings clinical trial data together in a clear, focused manner to drive smart decision-making processes.

  5. Data Management: Turning Data Into Insights 7/31/2025

    Turning Data into Insights

    At Catalyst Flex, we understand that clean data is the foundation of successful analyses. We are an accredited Medidata Partner and certified study builders in multiple platforms.

  6. The Asia Drug Development Advantage 8/8/2024

    Avance Clinical has located its Asia hub operations in Seoul, South Korea which is highly regarded for its advanced technology and scientific and medical excellence.

  7. Medical Writing Software 6/17/2025

    Accelerate Medical Writing Without Compromising Accuracy or Compliance

    In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.

  8. A QMS Software That Enhances Operational Excellence 3/24/2025

    Ideagen Quality Management is a modular SaaS solution designed with the needs of quality managers in mind. Trusted by more than 6,000 customers worldwide to digitalize their quality management processes and comply with industry standards.

  9. TrialKit eSource (Direct Data Capture) 6/6/2024

    Gain confidence in your clinical research data with direct data capture (DDC).

  10. Document Review Integrations And Technology Partners 6/18/2025

    At Ideagen, we're committed to empowering seamless collaboration and enhancing your document review process. Through strategic alliances with leading technology providers across the life science industry, we offer integrations that amplify the efficiency and effectiveness of your workflows.