Trial Management

  • Signant Health Partner Program

    Signant Health Partner Program

    Become a CRO partner today. Sponsors what to know what your competitive edge is, so let's show them. We'll make sure you are distinguished and trusted for delivering across the Signant portfolio.

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  • TrialConsent Self-Service and its Enablement

    TrialConsent Self-Service and its Enablement

    TrialConsent® Self-Service allows you to develop your own consent forms and documentation, create libraries for easy re-use across studies and maintain full control over your processes.

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  • Making eCOA Accessible for All Populations2:38

    Making eCOA Accessible for All Populations

    Elderly, children, people with disabilities, and everyone in between can use eCOA more effectively than paper in a clinical trial. Jery Grupp discusses why going electronic is preferred by sponsors.

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  • eCOA and Older Users: Users Prove that Age is Just a Number

    eCOA and Older Users: Users Prove that Age is Just a Number

    This document will set out CRF Health’s recommendations, provide an overview of best practices for eCOA in older users and offer considerations for implementation.

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  • eCOA Design Considerations: Reminders and Alarms3:46

    eCOA Design Considerations: Reminders and Alarms

    Dr. Jill Platko discusses why reminders and alarms are important for the simplest and most complex clinical trials, and how they can be used for optimal subject compliance.

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  • How Integrated Technology Benefits Patients and Investigators in Diabetes Clinical Trials

    How Integrated Technology Benefits Patients and Investigators in Diabetes Clinical Trials

    How Integrated Technology Benefits Patients and Investigators in Diabetes Clinical Trials

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  • Using eConsent in Clinical Research to Support Patient Understanding and Welfare

    Using eConsent in Clinical Research to Support Patient Understanding and Welfare

    Deciding to participate in a clinical trial is not risk-free for anyone. This article explores how to best support patients during the informed consent process (ICP) with eConsent.

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  • Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites1:02:32

    Electronic Informed Consent - 2017 Industry Survey Results from Clinical Sites

    In this webinar, CRF Health's Sandra "SAM" Sather is joined by Giga Smith from Coastal Carolina Healthcare (CCHC) to discuss Electronic Informed Consent (eConsent) from the research site perspective.

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  • Understanding the Benefits of eCOA in Oncology Clinical Trials13:18

    Understanding the Benefits of eCOA in Oncology Clinical Trials

    Dan Limbach of PharmaVOICE interviews CRF Health's Katie Garner, Therapeutic Areas Manager, about the benefits of using eCOA in oncology clinical trials.

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  • Validating Clinical Trial Data: Paper vs. eCOA2:50

    Validating Clinical Trial Data: Paper vs. eCOA

    Data integrity and validity have got to be the number one concern for anybody gathering data from subjects. Electronic Clinical Outcome (eCOA) solutions can help.

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  • How to Select Most Effective eCOA Modality for Your Study1:02:21

    How to Select Most Effective eCOA Modality for Your Study

    This webinar examines the electronic Clinical Outcome Assessment (eCOA) modalities available to clinical trials, such as handheld, tablet, web, Bring Your Own Device (BYOD), and mixed mode devices.

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  • Can Seniors Use eConsent?2:45

    Can Seniors Use eConsent?

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  • Managing eCOA Data - Principles and Best Practices

    Managing eCOA Data - Principles and Best Practices

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  • FDA Supports Innovation in Clinical Trials with eConsent4:12

    FDA Supports Innovation in Clinical Trials with eConsent

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  • 9 KPI Dashboards & Reports No eCOA Study Should Be Without

    9 KPI Dashboards & Reports No eCOA Study Should Be Without

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  • Reducing Regulatory Risk with eConsent3:14

    Reducing Regulatory Risk with eConsent

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  • Recruiting and Retaining Patients with eConsent3:28

    Recruiting and Retaining Patients with eConsent

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  • The Value of Electronic Informed Consent3:15

    The Value of Electronic Informed Consent

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  • 3 Ways Electronic Informed Consent Benefits Trial Participants3:59

    3 Ways Electronic Informed Consent Benefits Trial Participants

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  • How to Visualize Data to Increase Trial Performance and Efficiencies48:54

    How to Visualize Data to Increase Trial Performance and Efficiencies

    This live demo shows how new visualization tools in CRF Health’s TrialManager 6.0 enable monitoring of patients and sites in real time, resulting in lower clinical trial costs and higher data quality.

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