CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Partnership, merger, alliance, integration GettyImages-1019177936]( "Is Double Programming Really Required For Validation?")
Is Double Programming Really Required For Validation?Double programming has been the gold standard for validation, but technological advancements and improved sponsor oversight of CRO deliverables have introduced more efficient and reliable alternatives.
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![Checking prescription on smartphone-GettyImages-1719535353]( "Bring-Your-Own-Device For eCOA — Is It Worth It?")
Bring-Your-Own-Device For eCOA — Is It Worth It?At the recent SCOPE Summit, four experts in data management, monitoring, site operations, and tech weighed the pros and cons of adopting bring-your-own-device (BYOD) requirements for clinical trial eCOAs.
ECOA RESOURCES
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![GettyImages-1163698800 patient ePRO]( "What 4 Things Do All eCOA Studies Need To Succeed?")
Learn what else, in addition to good technology, study teams need for eCOA studies to succeed.
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![The New Era Of Evidence Generation In Clinical Trials]( "The New Era Of Evidence Generation In Clinical Trials")
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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![GettyImages-1363170016 wearables]( "The Future Of eCOA & Wearable Devices")
Learn how by looking at the advantages of wearables and where they are headed in the future, manufacturers, providers, and researchers can better anticipate collaboration efforts to bridge the gaps in existing processes and maximize the potential of eCOA wearables in clinical research.
ECONSENT RESOURCES
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![The New Era Of Evidence Generation In Clinical Trials]( "The New Era Of Evidence Generation In Clinical Trials")
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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![GettyImages-1346651718-decentralized-doctor-patient-computer-remote]( "Seamless And Integrated Onboarding For Trial Participants")
Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.
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![Preparing For eConsent - A Step By Step Guide For Site Personnel]( "Digital Medicine Society Accelerates Recruitment and Results With eConsent")
Find out how the Digital Medicine Society (DiMe), an interdisciplinary professional society for digital medicine, was able to deploy an eConsent module in less than two weeks to support its remote study to assess nocturnal scratching as an endpoint for patients.
EPRO RESOURCES
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![Professional employees discussing ideas of project on tablet pc iStock-836658296]( "Site Perspectives On BYOD ePRO Use")
This study examines participant convenience and compliance, aiming to understand and address the challenges faced by site personnel in global trials.
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![GettyImages-1413603540 doctor tablet]( "Paper vs. eCOA: Hard Calculations For Easy Decisions")
Sticker prices often guide purchases, but there's a broader perspective that encompasses total cost. Use this calculator to compare prices of paper COAs or eCOAs, including ePROs, eDiaries, and eClinROs.
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![FDAs Vision On PRO Collection For RWE]( "FDA's Vision On PRO Collection For RWE")
In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies, particularly in light of FDA expectations.
