CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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![GettyImages-1308685498]( "When The System Breaks, Who Pays? SCRS On Site Tech Gaps")
When The System Breaks, Who Pays? SCRS On Site Tech GapsSCRS CSSO Jimmy Bechtel on why clinical site tech integration is an architecture problem – and who bears the risk when remote systems fail.
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![scientist in a modern laboratory studies human body with HUD, graphic display-GettyImages-1396802026]( "HTA, Digital Twins, And Building Clinical Tech That Lasts")
HTA, Digital Twins, And Building Clinical Tech That LastsISPOR CEO Rob Abbott on HTA-integrated trial design, digital twin evidence gaps, SaMD’s continuous update problem, and the one change he’d mandate for clinical tech.
ECOA RESOURCES
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![GettyImages-1751848523-meeting-evaluation-charts-table]( "Accelerating CRO Study Deployment At Scale")
A top-3 CRO and a top-10 pharmaceutical company partnered with Medable to help accelerate, scale, and standardize their eCOA trials. See how they accomplished it.
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![Wearable iStock-1257436276]( "7 eCOA Design Recommendations: Insights From Sites And CRAs")
Signant joined a group of C-Path members including other eCOA solution providers, sponsors, and regulators for a GBTI project that revealed several opportunities to improve eCOA usability and flexibility.
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![iStock-1074203146-computer-typing-work]( "Setting A New Client Standard In Study Closeout Timelines")
Learn how a top-10 global pharmaceutical company achieved a significantly faster time to market for a high-profile therapy.
ECONSENT RESOURCES
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![dsg econsent snip thumb]( "Work Flow Walk Through: eConsent Platform")
Within DSG’s unified system, e-consent is simple. Witness how teams can easily and efficiently register participants for clinical trials.
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![GettyImages-1385471311 patient tablet]( "Revolutionizing Pediatric Clinical Trials With ePRO And eConsent")
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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![GettyImages-1159575307 econsent]( "A Better Approach To eConsent: Flexibility With Enabled Technology")
Electronic consent, or eConsent, digitalizes the trial participant consent process through increasingly simplified, interactive, educational models designed to improve comprehension and boost engagement.
EPRO RESOURCES
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![GettyImages-1385471311 patient tablet]( "Revolutionizing Pediatric Clinical Trials With ePRO And eConsent")
Digital tools like ePRO and eConsent are essential in addressing pediatric trial challenges such as the diverse participant ages and family involvement, which impact retention and data quality.
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![How Should Biosimilar Companies Approach Real-World Evidence?]( "Evidence Generation Evolved")
Explore how innovative strategies are cutting clinical trial times in half and accelerating the delivery of life-saving treatments.
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![GettyImages-870849774 EDC medrio]( "Reflexion Counts On Medrio To Launch First Studies")
Learn how a therapeutic oncology company was able to take advantage of an EDC system, establish a ePRO assessments collections platform, and receive guidance on data collection devices.
