Clinical Technologies Solutions

  1. TrialKit Engage For Televisits 12/29/2025

    Conduct secure video based visits, manage study schedules, and keep participants connected through a single unified platform.

  2. Rave Lite For Phase I Trials 9/12/2024

    Discover a flexible, cost-effective platform tailored to Phase I studies, providing rapid, efficient study builds, seamless transitions, and scalable solutions for early-stage clinical research.

  3. 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.

  4. 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.

  5. Introducing Sitetrove Global Patient Insights 5/15/2024

    With these insights, study sponsors can get a comprehensive view of the worldwide patient landscape, enabling the ability to locate sites with clinically relevant and diverse patient populations easily.

  6. Real World Data Solutions 12/16/2022

    Leverage Citeline RWD Solutions to enhance feasibility assessments, select optimal trial sites from the start and, when necessary, support trial rescue efforts.

  7. Cenduit Interactive Response Technology 4/25/2023

    Accelerate study start-up and amendments, simplify site and sponsor experience, reduce trial supply costs and improve study decision making while ensuring quality standards and patient safety during your trial with Cenduit Interactive Response Technology.

  8. Clinical Data Studio: Unlock The True Power Of Clinical Trial Data 1/5/2026

    Experience a transformative AI-powered data quality management solution that unifies study teams by providing seamless access to data from all clinical data sources.

  9. Unified, Integrated eClinical Research Solutions 1/16/2024

    Facilitate efficient digitalization and optimization of clinical trials that meet the unique needs of small and mid-size biopharma organizations with the Signant SmartSignals Unified Platform.

  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.