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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The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.
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![yprime ecoa webinar thumb]( "Patient-Focused Drug Development: eCOA Best Practices")
During this presentation, industry experts provide insights on how clinical trial stakeholders can enrich the participants' journeys in harmony with PFDD objectives.
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![rapid sculptor thumb]( "Rapid Study Design With The Sculptor Portal")
Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly.
ECONSENT RESOURCES
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![eConsent-Informed-tablet-iPad]( "How eConsent Can Help Legally Authorized Representatives")
Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.
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![GettyImages-1429594737 econsent]( "How Partnership Ensured A Successful First Digital Trial")
Discover how this collaborative approach and tailored recommendations led to the successful implementation of an eConsent tool for a kidney cancer study with U.S. Renal Care.
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![Accelerating Clinical Trials Through Streamlined Confidential Disclosure Agreements And Processes]( "Accelerating Clinical Trials Through Streamlined Confidential Disclosure Agreements")
In this presentation, Dr. Christine Senn addresses the persistent challenge of study startup delays by focusing on a primary legal hurdle: the Confidential Disclosure Agreement (CDA).
EPRO RESOURCES
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The shift from reporting on paper to reporting electronically has been happening for years, however, the transition hasn’t always been elegant. Explore how the pandemic has played a role in accelerating the shift to eCOA/ePRO.
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![IT Engineer Working in Monitoring Room-iStock-808157346]( "Safety Monitoring: What Does ePRO Have To Do With It?")
In the available blog post, learn about the importance of safety monitoring in clinical trials.
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![GettyImages-2036497686-lab-team-collaboration-laboratory-tablet-computer]( "Choosing The Right eClinRO Solution For Reliable Trial Data")
Electronic clinician-reported outcomes (eClinROs) enhance the quality and consistency of clinical trial data. Discover key factors to consider when selecting an eClinRO provider.
