CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Measuring-oxygen-saturation level-GettyImages-1392177599]( "Embracing Hybrid Trial Design — How, When, & Why To Use It")
Embracing Hybrid Trial Design — How, When, & Why To Use ItGlobal Clinical Sciences & Operations Innovation Lead Lewis Millen talks about UCB’s approach to hybrid trial design, how and when it chooses to implement remote and virtual elements, and why a hybrid trial is beneficial to both the sponsor and the patient.
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![treatment-technolocy-GettyImages-610451248]( "How PROs Enhance Patient Care Decisions And Future Clinical Research")
How PROs Enhance Patient Care Decisions And Future Clinical ResearchPatient-reported outcomes (PROs) offer unique insights that complement traditional treatment efficacy endpoints, such as survival or disease relapse, and can facilitate better discussions between clinicians and patients. When PROs are incorporated into clinical trial protocols, sponsors can gain a better understanding of the treatment’s impact from the patient’s perspective.
ECOA RESOURCES
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![GettyImages-1170544407 doctor value]( "The False Economy Of Paper Diaries In Clinical Trials")
While paper diaries may appear cheaper, but there are hidden costs that make a digital eCOA solution much more affordable in your clinical trial.
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![GettyImages-1337453095-doctor-patient]( "Direct-From-Patient Data Capture With eCOA")
Learn how an eCOA tool can provide patients a chance to be heard while giving sponsors quantitative and qualitative data to track the efficacy of a treatment.
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![GettyImages-1302453801 trial design ps]( "Considerations For Implementing The Best eCOAs In Your Trial Design")
Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
ECONSENT RESOURCES
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![GettyImages-1447084050 data]( "Gradually Investing In Direct Data Capture Is Inevitable")
Given study decentralization and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”
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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.
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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.
EPRO RESOURCES
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![GettyImages-1355941377 source data]( "Nevro Eliminates Majority Of Source Data Verification With ePRO And EDC")
Read how a global medical device company was able to unlock new efficiencies by implementing data collection via electronic patient-reported outcome assessments.
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![GettyImages-1302453801 trial design ps]( "Considerations For Implementing The Best eCOAs In Your Trial Design")
Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
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![Interview-with-Scott-Merz]( "Interview Mode: A Valuable Data Collection Alternative Supporting Decentralized Clinical Trials")
Download the available infographic to discover how collecting ePRO & eObsRO data via interview mode can be recommended in specific circumstances.
