CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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Sites Are Building Their Own Tech – SCRS On What That Means
SCRS’s Jimmy Bechtel on why Bring-Your-Own-Tech is both a protest and a performance differentiator, and what the industry needs to do about it.
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When The System Breaks, Who Pays? SCRS On Site Tech Gaps
SCRS CSSO Jimmy Bechtel on why clinical site tech integration is an architecture problem – and who bears the risk when remote systems fail.
ECOA RESOURCES
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In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.
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Real-time eCOA data enables faster eligibility decisions, proactive issue alerts, and streamlined operations by unifying data, improving precision, responsiveness, and trial execution efficiency.
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Projected to grow 16.1% annually through 2030, eCOA solutions are booming. Uncover the top five myths and misconceptions about eCOAs in 2025 so your clinical teams can make evidence-based decisions.
ECONSENT RESOURCES
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IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.
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Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
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Eliminate transcription errors and fully leverage supporting eClinical technology to provide a reliable consistent exchange of information.
EPRO RESOURCES
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Eliminate transcription errors and fully leverage supporting eClinical technology to provide a reliable consistent exchange of information.
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Discover how with the proper understanding of a site’s barriers, early engagement, and prioritizing effective training, site acceptance of ePRO can be improved.
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Bridge the gap between clinic and home with flexible data capture. Use any device to ensure consistent, real-time data entry and improve compliance throughout the study lifecycle.