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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![Clinical Tech Week]( "Enhance Data Collection And Ensure Seamless Platform Integration")
Discover how to enable patient- and site-centric data collection, enhance participant engagement, reduce burden, and deliver valuable real-world insights on treatment effectiveness and quality of life.
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![domino effect and risk management concept iStock-1272805554]( "eCOA Risk Management In The Digital Age")
Regulators across the globe are urging the industry to strengthen their data integrity practices. This article addresses the additional considerations that go hand in hand with the increased reliance on eSource data and the expansion of the electronic systems in clinical trials.
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![Business Globe Magnifier]( "Calling All Assessment Authors: Do You Want To Share Your COA With Sponsors Across The Globe?")
Explore how eCOAs will become an effective way to capture data remotely throughout the trial as sponsors shift to decentralized clinical trials.
ECONSENT RESOURCES
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![Medical data ipad iStock-1182616138]( "How eConsent Primes Patients And Studies For Success")
Understand how the informed consent process ensures trial participants are adequately educated about the trial and what's required of them during the process while confirming their willingness to enroll.
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![GettyImages-537316778 consent]( "How eConsent Is Changing The Informed Consent Process")
Learn how informed consent — providing a potential participant with enough information about a study to allow for an informed decision about their participation — is a critical step for enrolling patients in clinical trials.
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![castor video]( "Hybrid eConsent For On-Site Or Remote Patient Enrollment")
Castor’s suite of modular eConsent solutions creates clinical trial efficiencies from recruitment and screening, all the way to direct data capture and analysis.
EPRO RESOURCES
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![Clinical Tech Week]( "Enhance Data Collection And Ensure Seamless Platform Integration")
Discover how to enable patient- and site-centric data collection, enhance participant engagement, reduce burden, and deliver valuable real-world insights on treatment effectiveness and quality of life.
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![Doctor-Patient-Question-Network]( "Increasing The Usefulness Of PROs In Oncology Research")
Dr. Anthony Everhart (Clinical VP, Signant Health) and Tim Meyer (Professor, University College London) discuss opportunities for increasing the usefulness of PROMs.
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![castor epro webinar thumb]( "Exploring Modular Mobile And Web ePRO")
Review the capabilities of this collection of ePRO applications, available on both web and mobile platforms, for enhancing hybrid or decentralized clinical trial experiences.
