CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![Man facing complex problems-GettyImages-2224014902]( "Clinical Research Has System Sprawl Problem")
Clinical Research Has System Sprawl ProblemDisconnected systems are strangling clinical trials. Here’s what’s causing the sprawl, why it keeps getting worse, and what needs to change.
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![predictive medical analytics, digital AI interface, patient data, DNA insights-GettyImages-2262212753]( "How Clinical Trial Sites Must Adapt To The Predictive Analytics Era")
How Clinical Trial Sites Must Adapt To The Predictive Analytics EraClinical trial sites are now measured, ranked, and selected by predictive models. Learn how to perform and compete in this data-driven new era.
ECOA RESOURCES
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![China Globe World]( "5 Key Considerations For Implementing Digital Technologies To Support Patients In China")
In this post, gain insight into five key considerations that will help support patients in China.
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![GettyImages-623208264 lab, research, oncology]( "eCOA In Oncology Trials: A Tool To Simplify")
Accurate quality of life data is critical in oncology. eCOA unified with IRT streamlines trials, improves data collection, and enhances site user experiences across therapeutic areas.
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![Patient-Centricity: A Progressive Prescription For Modern Healthcare]( "eCOA And Digital Platforms Reduce Diabetes Study Startup To 8 Weeks")
See how digital solutions came together to enable faster study startup by 50% for this top pharma company conducting a Phase 3 diabetes study within the weight loss market.
ECONSENT RESOURCES
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![iqvia complete consent thumb]( "Unleash The Power Of IQVIA Complete Consent")
Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
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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.
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![GettyImages-2181934436-laboratory-analysis-scientists-technology-computer]( "Virtual eConsent For Decentralized Trials")
Virtual eConsent improves accessibility and compliance in decentralized trials, streamlining enrollment with a secure, user-friendly process for informed consent in remote research.
EPRO RESOURCES
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![GettyImages-2036497698 clinical lab]( "Solutions For Sponsors Utilizing Drafted Guidance For PROs In Oncology")
Explore the challenges pharmaceutical companies face in implementing PROs in cancer clinical trials as outlined in the FDA’s draft guidance, as well as strategies to overcome these obstacles.
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![medrio snip thumb]( "An ePRO Platform Designed With Real People In Mind")
With a combination of technology and consultative support from team experts, start experiencing a seamless ePRO transition and establish a smoother path to regulatory submission today.
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![eConsent-Informed-tablet-iPad]( "Minimizing Hurdles For Patients During The eConsent Process")
Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.
