CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Edge computing 873875560]( "Edge AI Is Reshaping How Clinical Trials Run")
Edge AI Is Reshaping How Clinical Trials RunEdge computing and AI are transforming clinical trials – enabling real time monitoring, decentralized research, and faster, more cost-effective drug development.
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![GettyImages-1208552262 elderly, patient, telehealth]( "Telehealth In Clinical Trials: What Sites And Patients Think")
Telehealth In Clinical Trials: What Sites And Patients ThinkSites and patients have complicated views on telehealth in trials. Here’s what the evidence shows about who benefits, who bears the burden, and where the limits are.
ECOA RESOURCES
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![GettyImages-653836738 data researcher]( "Shaping The Future Of eCOA User Acceptance Testing")
Proactive planning by sponsors and early User Acceptance Testing (UAT) involvement in the eCOA design process can substantially improve study quality, efficiency, and consistency.
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![GettyImages-1443965506 doctor clinical trial data monitoring]( "Optimizing Prader-Willi Syndrome Clinical Trials")
Learn how Signant is helping to mitigate placebo responses and ensuring high-quality data to improve Prader-Willi syndrome (PWS) clinical trial success.
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![GettyImages-2161842577-business-professional-laptop-office-table]( "Unified Technology To Streamline Clinical Trials")
Connect every step of the trial journey with patented data-level integration that links sponsors, sites, and patients.
ECONSENT RESOURCES
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![medable econsent webinar]( "Agile eConsent: Taking A Flexible Approach To Global Implementation")
Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.
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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.
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![irb-submissions]( "How To Prepare An IRB Submission For A Remote eConsent Study")
IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.
EPRO RESOURCES
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![GettyImages-1355166705 ePRO]( "3 Steps To Improve Site Acceptance Of ePRO In Medical Device Trials")
Discover how with the proper understanding of a site’s barriers, early engagement, and prioritizing effective training, site acceptance of ePRO can be improved.
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![GettyImages-1065782758 migraine]( "Training Program Reduces Placebo Effect By More Than 50% In ePRO Study")
Discover how an instruction program directly contributed to significantly lowering the placebo response rate in a phase III migraine CNS study.
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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.
