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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![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.
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![top 5 myths about eCOA]( "The Top 5 Myths About eCOAs In 2025")
Join leading clinical experts as they debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions.
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![Clinical Tech Week]( "The AI-Native Platform For Modern Clinical Research")
Join Curebase CEO Tom Lemberg for a live demo of our next-generation ePRO/eCOA technology. See how our AI Assistant lets you build forms, generate translations, and enter data in seconds with our intuitive, user-friendly platform.
ECONSENT RESOURCES
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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.
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![GettyImages-2184303900- medica-2025-edc]( "The Transformative Impact Of EDC Systems In 2025")
The shift towards decentralized and hybrid trials underscores the significance of EDC in expanding geographic reach, fostering diversity in participant populations, and reduce participant burden.
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![person using ipad iStock-1029343476]( "Re-Consent In Clinical Trials: Streamlining With eConsent")
Delve into a variety of triggers for initiating re-consent, perspectives of regulators and IRBs regarding the re-consent process, and the role of digital processes in preventing issues related to re-consent.
EPRO RESOURCES
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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.
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![GettyImages-2184303900- medica-2025-edc]( "The Transformative Impact Of EDC Systems In 2025")
The shift towards decentralized and hybrid trials underscores the significance of EDC in expanding geographic reach, fostering diversity in participant populations, and reduce participant burden.
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![FDAs Vision On PRO Collection For RWE]( "FDA's Vision On PRO Collection For RWE")
In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies.
