CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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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.
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![decisions, pick the right path-GettyImages-2156909134]( "Pick The Right PV Technology With Help From A Safety Data Management Expert")
Pick The Right PV Technology With Help From A Safety Data Management ExpertOtsuka's Head of U.S. GPV Safety Data Management Vikalp Khare shares how smart governance should inform pharmacovigilance (PV) technology choices.
ECOA RESOURCES
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![GettyImages-1499371064-money-sign-cost-rising-graph]( "The Real Cost In CNS Trials: Rater Drift And Site Readiness")
Learn how to build resilience into CNS trial operations with evidence-based frameworks that prioritize human factors alongside digital tools.
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![Kayentis DCT webinar]( "Are You Ready For Fully Remote eCOA In Your Next DCT Trial?")
Watch to learn how you can build a better data management and compliance monitoring plan for your COAs in your next DCT trial.
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![GettyImages-1133924836 software]( "How SaaS Unlocks New Possibilities For Life Science Organizations")
The rise of SaaS (software-as-a-service) has transformed industries, including life sciences, by enabling new possibilities. See how it’s already helping life science organizations around the world today.
ECONSENT RESOURCES
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![iqvia tech snip 2 thumb]( "Successful Subject Creation With eCOA, eConsent, & IRT Process Flow")
Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.
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![veeva clinical platform thumb]( "End-To-End Clinical Data Flow")
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.
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![GettyImages-1483191270 patient]( "Waiver Of Consent vs Waiver Of Written Consent")
Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.
EPRO RESOURCES
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![GettyImages-672689894 oncology trial]( "Ensuring Patient-Centered Care In Oncology Trials")
In oncology trials, safety and tolerability are a core focus. From centralized ECGs to patient-reported outcomes, utilize this guide for optimizing assessments of drug safety and quality of life.
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![African student guy sit at desk hold papers-iStock-1253877173]( "Paper Vs ePRO: Clinical Data Collection Methods")
Patient-reported outcomes (PROs) assess patients' health without clinician interpretation. Traditional paper methods often result in missing data and quality issues, while electronic solutions enhance data accuracy and completeness.
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![veeva clinical platform thumb]( "End-To-End Clinical Data Flow")
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.
