CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Medical research, technology, innovation, AI-GettyImages-2226144959]( "The Site Perspective: Why Ambient AI Is The Missing Link In Clinical Trial Data Integrity")
The Site Perspective: Why Ambient AI Is The Missing Link In Clinical Trial Data IntegrityDiscover how AI ambient listening has changed the way Mikel Daniels, DPM, MBA, and his team conduct clinical research at WeTreatFeet Podiatry.
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![Cybersecurity, digital connection, digital safety-GettyImages-2123163641]( "Penetration Testing In Healthcare: Common Vulnerabilities And Programs To Address Them")
Penetration Testing In Healthcare: Common Vulnerabilities And Programs To Address ThemExplore some of the common pitfalls witnessed in healthcare environments, as well as guidance for implementing a penetration testing program.
ECOA RESOURCES
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![Cancer Social Network]( "A Leading Academic Medical Center Monitors Newly Diagnosed Myeloma Patients")
Learn how eCOA helped to motivate patients and increased engagement around experiences outside of the clinical setting, which otherwise may have gone unmentioned.
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![Signant Health Performance Data thumb]( "Signant StudyIQ Trial Management Suite Overview")
See how our dynamic and rich reporting solutions facilitate high-quality clinical data and support efficient trial management. All reports, dashboards, and analytics come standard with our eCOA solutions.
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![Notifications And Reminders]( "Notifications And Reminders")
Configurable alarms appear as banner alerts on subjects’ devices, while email notifications help sites monitor potential non-compliance and respond to newly uploaded symptom severity data.
ECONSENT RESOURCES
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![GettyImages-1385471311 patient tablet]( "Revolutionizing Pediatric Clinical Trials With ePRO And eConsent")
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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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.
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![Patient with ipad]( "How eConsent Delivers Value For Sponsors")
Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.
EPRO RESOURCES
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![GettyImages-1385471311 patient tablet]( "Revolutionizing Pediatric Clinical Trials With ePRO And eConsent")
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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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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![Disruption Mobile]( "Simplifying ePRO Data Collection")
The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.
