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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![GettyImages-1294781200 artifical intelligence]( "A New Approach To Faster Electronic Clinical Outcome Assessment (eCOA) Development")
The value of eCOA tools is undisputed, but using a waterfall methodology of software delivery is highly inefficient. Explore how a more agile approach to eCOA development can produce a fully functional eCOA in a day.
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![Medable eCOA webinar]( "Transforming Oncology Trials With Next-Gen eCOA")
With the FDA stating last fall that the “patient’s voice” is key to understanding real-world-impacts, eCOAs and ePROs are becoming quintessential tools for cancer trials.
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![Telehealth Remote Clinical Trial]( "Televisits: Why Integrate Telemedecine Features In eCOA Trials?")
Discover new possibilities where patients can complete several of their clinical study procedures remotely, making their participation in clinical trials easier and less cumbersome than site-based trials.
ECONSENT RESOURCES
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![iStock-919825866-patient-doctor-education-counsel]( "Better eConsent Through Education Best Practices")
eConsent can have a positive impact on participant retention, but learn why that is only part of the challenge of meeting participant needs in a clinical trial.
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![GettyImages-1159575307 econsent]( "A Better Approach To eConsent: Flexibility With Enabled Technology")
Electronic consent, or eConsent, digitalizes the trial participant consent process through increasingly simplified, interactive, educational models designed to improve comprehension and boost engagement.
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![castor vid snip thumb]( "Efficiently Manage Clinical Data With Castor's EDC, CDMS")
Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.
EPRO RESOURCES
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![Medable eCOA webinar]( "Transforming Oncology Trials With Next-Gen eCOA")
With the FDA stating last fall that the “patient’s voice” is key to understanding real-world-impacts, eCOAs and ePROs are becoming quintessential tools for cancer trials.
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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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![veeva rethinking epro thumb]( "Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials")
Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials.
