CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Business woman looking at laptop-GettyImages-503422576]( "Why Patients Drop Out And How To Stop Them")
Why Patients Drop Out And How To Stop ThemFrom scheduling friction to silent financial stress, patient dropout derails trials. Here’s what’s causing it and the tech helping sites fight back.
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![medical analytics, digital AI interface, DNA insights, machine learning, healthcare-GettyImages-2262212754]( "Predictive Analytics Is Reshaping How Sponsors Run Clinical Trials")
Predictive Analytics Is Reshaping How Sponsors Run Clinical TrialsPredictive analytics is transforming clinical trial operations, from enrollment forecasting to risk-based monitoring. Here’s what sponsors need to know.
ECOA RESOURCES
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![GettyImages-1212803649-covid-virus-vaccine]( "Fighting COVID-19 Like A Pro")
Explore how the use of electronic Clinical Outcomes Assessments (eCOAs) can be rapidly implemented to capture patient reported outcomes (PROs).
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![parkinson]( "Recentering Parkinson's Disease Trials On Patients")
This ebook describes how electronic clinical outcomes assessments (eCOA), mobile digital assessments, and other innovative data capture technologies are able to “meet patients where they are” in Parkinson’s Disease trials – with increasingly objective, sensitive, and continuous measures.
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![GettyImages-868669738 eCOA]( "eCOA Solution Design Recommendations: Applied Insights From Trial Sites, CRAs")
Enhance hybrid trials with digitalization through remote data capture using smartphones, tablets, and computers, improving participant experience and data integrity.
ECONSENT RESOURCES
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![eConsent-Informed-tablet-iPad]( "Minimizing Hurdles For Patients During The eConsent Process")
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
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![GettyImages-1322205575 data ps]( "EDC For Mid-Study Changes In Medical Device Clinical Trials")
In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.
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![GettyImages-182487080 FDA]( "Unlocking The Power Of Real-World Evidence In FDA Submissions")
Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.
EPRO RESOURCES
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![eConsent-Informed-tablet-iPad]( "Minimizing Hurdles For Patients During The eConsent Process")
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
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![Patient Reported Outcome ePRO]( "How To Overcome The Problem Of The Early ePRO Oversell")
In this blog, explore how the approach to PROs needs to be reconsidered, given increasing regulations and trial scrutiny, the clinical need for patient-reported outcomes, and the ability to drive costs down and move off paper.
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![GettyImages-1081947082 clinical technology]( "Increase Participant Diversity With eClinical Tools")
The right technology and community partnerships can help sponsors meet FDA diversity requirements without additional expenditures, build relationships with minorities, and prepare for future trials.
