CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
-
![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.
-
![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
-
![GettyImages-1729747338-2024-evolution-growth]( "Solving Key eCOA Challenges Through Digital Trials—Proof Points!")
Medable has reached some important milestones and shares them in its end-of-year report. Check it out to see what game-changing results they've brought to their customers.
-
![GettyImages-953449116 clinical trial oversight]( "Can Your Clinical Trial Design Handle Mid-Study Changes?")
Mid-study changes are frequently inevitable, but it’s possible to reduce the downtime they create with strategic planning and technology. See how to plan for mid-study changes that mitigate downtime.
-
![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.
ECONSENT RESOURCES
-
![GettyImages-1137736725 data platform]( "Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study")
This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.
-
![GettyImages-1314299046 econsent]( "Preparing Studies With eConsent For IRB Approval")
Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.
-
![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.
EPRO RESOURCES
-
![GettyImages-1137736725 data platform]( "Achieving A 2.67x Reduction In Study Build Time For An Innovative Neuromodulation Study")
This study explores the potential of Focused Ultrasound Neuromodulation in deepening meditative states, and the platform that helps enhance the overall experience for researchers and participants alike.
-
![GettyImages-1483104506 Document Digitization Concept]( "eCOA 101: Why Choose ePRO vs. Paper")
ePRO solutions enhance data quality, operational efficiency, and patient-centricity in clinical trials by allowing patients to report outcomes digitally instead of using pen and paper.
-
![GettyImages-953449116 clinical trial oversight]( "Can Your Clinical Trial Design Handle Mid-Study Changes?")
Mid-study changes are frequently inevitable, but it’s possible to reduce the downtime they create with strategic planning and technology. See how to plan for mid-study changes that mitigate downtime.
