Clinical Technologies Solutions

  1. 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.

  2. 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.

  3. The SaaS Clinical Data Science Platform 4/8/2024

    Signals Clinical streamlines clinical data workflows, reducing the time spent preparing data for analytics. Its comprehensive platform enables the rapid delivery of clinical insights that inform both clinical and operational study decisions.

  4. Selecting And Evaluating An eRegulatory Solution 10/6/2023

    Take advantage of this checklist for evaluating eRegulatory solutions for clinical trial offices.

  5. Modernize Clinical Research With Continuous Digital Data 9/11/2025

    Modernize clinical research with a unified digital platform that collects continuous, high-precision data to provide meaningful discovery in clinical trials.

  6. 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.

  7. Elevating The Site Voice And Partnering For Patients 6/18/2024

    Discover how Medidata empowers clinical research sites with intuitive, unified technology solutions, elevating site voices and streamlining workflows to enhance patient care and research outcomes.

  8. Streamline Your Regulatory Process 1/18/2022

    The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.

  9. Standardized Data In One Place 1/27/2025

    Simplify clinical trial data management with Signant’s Clinical Data Hub. Harness machine learning to aggregate diverse data sources, streamline analysis, and unlock timely, actionable insights.

  10. Accelerate Your Operations With Smarter Trial Management 1/22/2025

    Learn about a cloud-based solution that centralizes clinical and operational data to improve the efficiency and oversight of clinical trials.