Featured Articles

Signant Health thought leadership from around the digital world

  • Building Patient Engagement and Secure Drug Discovery - Data Privacy, Compliance, and Security

    Building Patient Engagement and Secure Drug Discovery - Data Privacy, Compliance, and Security

    Much has been made of the trials and tribulations of complying with data regulations; however, Paul Drake from Signant argues there may be significant opportunities to be gained from data compliance

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  • Delving into eConsent: Industry Survey Reinforces Patient Centricity

    Delving into eConsent: Industry Survey Reinforces Patient Centricity

    Signant conducted an electronic informed consent (eConsent) survey to obtain insights from sponsors and CROs. Here are the findings from this key piece of research

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  • PharmaVoice -  Leveraging Virtual Technology to Improve Processes

    PharmaVoice - Leveraging Virtual Technology to Improve Processes

    In this issue of PharmaVoice, Signant Health's Bill Byrom shares his viewpoint of the potential of virtual health.

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  • Wear it on Your Sleeve — How Sensors and Wearables Help Drive Richer Insights on Intervention Effects

    Wear it on Your Sleeve — How Sensors and Wearables Help Drive Richer Insights on Intervention Effects

    As previously featured in PharmaVoice, Bill Byrom shares how the use of sensors and wearables in clinical trials can help replace the subjectivity of eCOA data collected with objective, accurate data.

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  • The Changing Face of Oncology Endpoint Monitoring

    The Changing Face of Oncology Endpoint Monitoring

    Oncology trials have always relied on tumor response to gauge efficacy. But in a world of patient-centricity and value-based reimbursement, do these "hard endpoints” the whole story?

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  • Successful Oncology Trials Need Intelligent Supply Management

    Successful Oncology Trials Need Intelligent Supply Management

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  • eConsent Tearing Down Barriers to Oncology Trials

    eConsent Tearing Down Barriers to Oncology Trials

    Journal for Clinical Studies Article: eConsent: Tearing Down Barriers to Oncology Trials, co-authored by Neetu Pundir & Bill Byrom, Signant Health.

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  • Power of Mobile Technology to Optimize Patient Engagement

    Power of Mobile Technology to Optimize Patient Engagement

    Power of Mobile Technology to Optimize Patient Engagement and Study Success, article, authored by Neetu Pundir, Signant Health, published in the Journal for Clinical Studies.

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  • The Case for Integrated IRT

    The Case for Integrated IRT

    An integrated just-in-time interactive response technology (IRT) interface can help companies reduce the costs of maintaining adequate buffers in their clinical supply chain.

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  • ePRO for the Modern Trial: Considerations to Implementing a BYOD or Partial Provisioning Strategy

    ePRO for the Modern Trial: Considerations to Implementing a BYOD or Partial Provisioning Strategy

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  • Improving Outcomes in Diabetes Research

    Improving Outcomes in Diabetes Research

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  • Improving-patient-outcomes-eCOA-cancer

    Improving-patient-outcomes-eCOA-cancer

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  • Leveraging Technology to Develop New Trial Endpoints

    Leveraging Technology to Develop New Trial Endpoints

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  • eConsent Regulatory Myths_PME_NPundir

    eConsent Regulatory Myths_PME_NPundir

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  • Optimizing Outcomes - Reduce the Burden of Data Collection - Oncology

    Optimizing Outcomes - Reduce the Burden of Data Collection - Oncology

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  • An IRB Perspective on Improving Informed Consent

    An IRB Perspective on Improving Informed Consent

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  • What the Future Holds for Informed Consent

    What the Future Holds for Informed Consent

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  • Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption

    Recruitment & Retention: Breaking Down the Barriers to eConsent Adoption

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  • In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

    In Pursuit of eConsent: Best Practice Recommendations for Successful Integration

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  • eConsent: 5 Key Areas of Preparation

    eConsent: 5 Key Areas of Preparation

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