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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![iPad-Medical-Remote-Digital-iStock]( "Simplify Your Clinical Data Flow To Streamline And Automate Modern Data Review")
Examine the three reasons why simplifying your clinical data flow can increase operational oversight, shorten data management cycle times, and reduce the manual burdens on data management teams.
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![How To Spec, Purchase, And Implement The Right IRT System For Your Clinical Trial]( "Ready For Remote: eCOA Adapts To A Hybrid World")
Due to the global health impact of COVID-19, many aspects of daily life have been moved to a hybrid model, meaning a mix of in-person and technology-enabled interactions In this blog, learn why eCOAs are especially well-suited for hybrid clinical trials.
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![Bright -ideas- innovation- inspiration-GettyImages-1371712788]( "How Small And Mid-Sized Biopharmaceutical Companies Can Easily Achieve Digital Innovation For Their Clinical Data")
Discover how forward- thinking life science companies are defining their vision and looking for like-minded partners to execute information technology.
ECONSENT RESOURCES
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![Patient with ipad]( "A Definitive Guide To Evidence Generation")
Obtain a complete understanding of enrollment, screening, consent, and data collection by diving into this introductory handbook on decentralized clinical trials.
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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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![EU-european-union-flag-map]( "EU Annex 11: How To Stay Compliant")
EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11.
EPRO RESOURCES
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![GettyImages-1499160012-patient-paperwork-clipboard-waiting-room-doctor-office]( "Strategies To Minimize Participant And Healthcare Provider Burden")
Patient-reported outcomes (PROs) are vital for clinical trials but can burden participants and providers. Discover strategies and practical solutions to ease these burdens and improve data quality.
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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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![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.
