Featured Products & Services

31. Decentralized Clinical Trials: The Future Of Clinical Research 9/26/2022

    Our integrated EDC platform, including eConsent, ePRO, RTSM, and DDC, is your gateway to decentralized trials. 

32. Simulants: Unlock Insights And Accelerate Medical Breakthroughs 11/17/2023

    Get an overview of this groundbreaking synthetic data product – uniquely derived from Medidata’s exclusive repository of global, standardized historical clinical trial data.

33. Medrio eConsent 10/5/2023

    Flexible consent technology improves participant comprehension and process oversight. Learn how Medrio’s eConsent solution is empowering organizations to accelerate all aspects of the consent process.

34. Flexible Solutions To Facilitate Comprehension And Compliance 9/18/2024

    Effective consent goes beyond signatures. Learn how to enhance participant understanding, streamlines document management, and improve workflow efficiency, to reduce errors and inspection risks.

35. ePRO For Oncology Studies 5/15/2024

    Now introducing a customized ePRO solution designed specifically for oncology studies: a user-friendly app with a streamlined two-step onboarding process.

36. 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.

37. Medrio eCOA/ePRO 10/10/2023

    Learn how teams can enhance data quality, engagement, and retention through this affordable and patient-focused approach.

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

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

39. ePRO: Capture Data At The True Source 9/25/2024

    Learn more about the successful compliance rates achieved with Castor Connect, as well as how you can maximize your data capture, simplify site actions, and reduce your workload.

40. Hybrid eConsent: Remote And On-Site 3/21/2025

    Studies show when participants are informed and comfortable with the consent process, they're more likely to comply with protocol, remain enrolled, and contribute to faster study deployment.