Blogs / Vlogs

  • Signant Health Raises the Bar in Ulcerative Colitis Trials with eCOA

    Signant Health Raises the Bar in Ulcerative Colitis Trials with eCOA

    Q&A with Katie Garner, Signant Health: Using eCOA in Ulcerative Colitis Trials for Seamless MAYO Score Calculation

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  • DIA 2019:  PharmaVOICE Interview with Mike Nolte, CEO, Signant Health10:31

    DIA 2019: PharmaVOICE Interview with Mike Nolte, CEO, Signant Health

    DIA 2019: PharmaVOICE interview with Mike Nolte, CEO Signant Health.

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  • Signant Health Unveiled at DIA 2019

    Signant Health Unveiled at DIA 2019

    DIA 2019 Recap by Signant Health.

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  • Electronic Version of the Neurostatus-EDSS Improves MS Trials

    Electronic Version of the Neurostatus-EDSS Improves MS Trials

    University Hospital Basel, Novartis and Signant Health (formerly CRF Health) recently published our experience data on the use of the eEDSS obtained from two phase III Multiple Sclerosis trials.

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  • Patient-Centric Technology in Clinical Trials: A Recap

    Patient-Centric Technology in Clinical Trials: A Recap

    A recap of our inaugural CRF Bracket Patient-Centric Technology in Clinical Trials roadshow in Boston.

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  • Different, Not Less: Why We Need to Ensure Clinical Research is Patient-Driven

    Different, Not Less: Why We Need to Ensure Clinical Research is Patient-Driven

    In honor of Autism Awareness Month, we spoke with Brian Catton, PharmD, who he sheds light on Autism and awareness surrounding the disorder.

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  • Leveraging Technology to Develop New Trial Endpoints

    Leveraging Technology to Develop New Trial Endpoints

    Technology is enabling us to provide richer insights and potentially measure new meaningful constructs in clinical trials that we have been unable to assess robustly in the past.

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  • Leveraging Today's Gaming For Better Health Reported Outcomes Tomorrow - ICDVRAT 2018

    Leveraging Today's Gaming For Better Health Reported Outcomes Tomorrow - ICDVRAT 2018

    Researchers from across the world collaborated to review work developing applications using immersive and mobile technologies as clinical treatment options, or as a means of objectively measuring and

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  • Seven Ways eCOA will Improve Your CNS Clinical Trials

    Seven Ways eCOA will Improve Your CNS Clinical Trials

    Capturing Clinical Outcomes Assessments in CNS studies can be difficult due to the unique patient populations in this therapeutic area. eCOA has emerged as the preferred method of capturing patient da

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  • Must Read Book for Researchers Implementing ePRO

    Must Read Book for Researchers Implementing ePRO

    This book is intended to provide information on the successful design and implementation of electronic patient-reported outcomes (ePRO / eCOA) in pharmaceutical clinical trials and clinical research.

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  • Simplifying the Implementation of Electronic Patient-Reported Outcomes - Applied Clinical Trials

    Simplifying the Implementation of Electronic Patient-Reported Outcomes - Applied Clinical Trials

    There have been a number of significant scientific and regulatory milestones driving the adoption of electronic patient-reported outcomes (ePRO) in clinical trials since 1980.

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  • Game Technology Opens New Path to Clinical Endpoints - DIA Podcast

    Game Technology Opens New Path to Clinical Endpoints - DIA Podcast

    Dr. Bill Byrom, VP of Product Strategy & Innovation at CRF Health discusses the future of electronic patient reported outcomes (ePRO), mobile accelerometry, & other mobile devices, in clinical trials.

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  • Preparing for eConsent - A Step by Step Guide for Site Personnel

    Preparing for eConsent - A Step by Step Guide for Site Personnel

    5 steps to help sites prepare for implementing an electronic informed consent (eConsent) solution.

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  • Patient-Centric Research Involving Patients in Clinical Trials Can Lead to Better Outcomes

    Patient-Centric Research Involving Patients in Clinical Trials Can Lead to Better Outcomes

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  • Reducing Patient Challenges of Data Collection During Oncology Clinical Trials

    Reducing Patient Challenges of Data Collection During Oncology Clinical Trials

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  • 10 Steps for Successful Migration of COA from Paper to Electronic

    10 Steps for Successful Migration of COA from Paper to Electronic

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  • Benefits of a Combined eCOA/eConsent Solution

    Benefits of a Combined eCOA/eConsent Solution

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  • Understanding the EMA Oncology PRO Guideline Appendix – We Can Help!

    Understanding the EMA Oncology PRO Guideline Appendix – We Can Help!

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