CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![scientist in a modern laboratory studies human body with HUD, graphic display-GettyImages-1396802026]( "HTA, Digital Twins, And Building Clinical Tech That Lasts")
HTA, Digital Twins, And Building Clinical Tech That LastsISPOR CEO Rob Abbott on HTA-integrated trial design, digital twin evidence gaps, SaMD’s continuous update problem, and the one change he’d mandate for clinical tech.
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![Man with smart ring-GettyImages-2218451704]( "Real-World Evidence And Wearables Are Reshaping Trial Tech")
Real-World Evidence And Wearables Are Reshaping Trial TechISPOR’s Rob Abbott on why RWE moved to number two in the 2026-2027 HEOR Trends Report, and what wearables, data fragmentation, and HARPER+ mean for clinical platforms.
ECOA RESOURCES
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![yprime ecoa webinar thumb]( "Patient-Focused Drug Development: eCOA Best Practices")
During this presentation, industry experts provide insights on how clinical trial stakeholders can enrich the participants' journeys in harmony with PFDD objectives.
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![technology]( "Three Benefits Of Centralizing Global Content For eCOA Migration")
Now, more than ever, sponsors aim to empower the global patient voice through patient-centric technologies—including providing wearable technologies and using electronic clinical outcome assessments (eCOAs) to collect patient data.
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![GettyImages-1390654899 esource patient]( "How Capturing Data Directly Is Transforming Trials")
With the right eSource technology, discover how trial data can be aggregated, integrated, and classified to accelerate data analysis for insight-based decisions in real time.
ECONSENT RESOURCES
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![GettyImages-1390654899 esource patient]( "How Capturing Data Directly Is Transforming Trials")
With the right eSource technology, discover how trial data can be aggregated, integrated, and classified to accelerate data analysis for insight-based decisions in real time.
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![GettyImages-1648451225 Scientist holding tray of samples in laboratory]( "Introducing Digitally-Enabled Biosample Consent Storage")
Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation of informed consent for centrally stored biospecimens.
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![eConsent-Informed-tablet-iPad]( "How eConsent Can Help Legally Authorized Representatives")
Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.
EPRO RESOURCES
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![GettyImages-1346698461 workflows]( "Rose Research Center Leans On Medrio To Simplify Workflows And Study Design")
After experiencing paper processing issues, discover how a company transitioned to digital data collection by using Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) solutions.
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![GettyImages-539843648 regulations doctor]( "Regulatory Guidance For PRO Strategy In Oncology Trials")
Kelly Dumais, Principal Scientific Advisor, and Jowita Marszewska, Scientific Advisor at Clario eCOA, delve into the specifics of how recent regulatory advancements are influencing PRO Strategy.
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![castor paper epro webinar thumb]( "From Paper To ePRO: Providing Flexibility And Efficiency")
Explore the transformative impact of flexible ePRO technology on clinical trials, elucidating how it enhances patient-centricity and operational efficiency for sponsors.
