CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![artificial intelligence regulation, legal compliance, digital governance, corporate transparency technology-GettyImages-2261879463]( "What Is Shadow AI, And How Does It Impact Clinical Trial Tech?")
What Is Shadow AI, And How Does It Impact Clinical Trial Tech?Discover how shadow AI appears in clinical trial technology and learn how to develop a practical control plan that protects participants and data without slowing innovation.
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![virtual line connecting strategy vision plan business ideas-GettyImages-1153174099]( "Building A Clinical Trial Tech Stack That Actually Works")
Building A Clinical Trial Tech Stack That Actually WorksThe right clinical trial tech stack isn’t the most complete one; it’s the one built with sites, funded fairly, and designed to remove friction, not add it.
ECOA RESOURCES
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![Japan Globe]( "Building A Gold Standard Trial Experience In Japan")
Hear how Medable worked with a Japanese sponsor to elevate their trial experience, achieve >90% patient and site adherence, and beat their forecasted FPI date, creating new eCOA standards adopted across all the customer’s vendors.
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![Medable ceo 2]( "Letter From The CEO: A New Era Of Drug Development Is Here")
This letter from Medable CEO Michelle Longmire lays out why we created Studio, what it enables sponsors and CROs to do, and how it will help everyone bring more effective therapies to patients faster.
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![Emotions-iStock-471812192]( "The Case For Cognitive Assessments In Phase 1 Clinical Trials")
Regulators prioritize patient-reported outcomes. Cognitive assessments in Phase 1 trials detect early drug-related cognitive effects, ensuring safety and efficacy. Signant’s CDR System® is a proven tool for this.
ECONSENT RESOURCES
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![Laptop clinical trials iStock-653839742]( "What Are Decentralized Clinical Trials (DCTs)?")
Discover how DCTs leverage “virtual” tools, such as telemedicine, sensory-based technologies, wearable medical devices, and direct delivery of study drugs and materials to patients’ homes.
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![COVID 19 Coronavirus Mask Wearer]( "Our Unified Platform Serves As eSource For COVID Treatment Trial")
Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.
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![GettyImages-1354589551 Documentation Management]( "Supporting Early Phase Oncology Research With The Right Data Management System")
Better understand how the evolving landscape drives innovation, why your data capture strategy needs the right technology foundation, and what to look for in a CDMS/EDC system for early-phase oncology.
EPRO RESOURCES
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![The impact of ePRO on the patient & site journeys]( "ePRO's Impact On Patient And Site Journeys")
Join our solutions experts as they demonstrate how Castor ePRO can enhance your clinical trial by improving the patient experience and streamlining site operations.
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![GettyImages-1346698461 workflows]( "Rose Research Center Leans On Medrio To Simplify Workflows And Study Design")
After experiencing paper processing issues, discover how a company transitioned to digital data collection by using Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) solutions.
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![GettyImages-1413603540 doctor tablet]( "Paper vs. eCOA: Hard Calculations For Easy Decisions")
Sticker prices often guide purchases, but there's a broader perspective that encompasses total cost. Use this calculator to compare prices of paper COAs or eCOAs, including ePROs, eDiaries, and eClinROs.
