CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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HTA, Digital Twins, And Building Clinical Tech That Lasts
ISPOR 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.
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Real-World Evidence And Wearables Are Reshaping Trial Tech
ISPOR’s Rob Abbott on why RWE moved to number two in the 2026-2027 HEOR Trends Report, and what wearables, data fragmentation, and HARPER+ mean for clinical platforms.
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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Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.
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Learn how to streamline the collection of essential data, thus alleviating patient burdens, all the while upholding data integrity within a flexible trial environment.
ECONSENT RESOURCES
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See how a team of four managed data for 40 peer-reviewed studies and 200,000 participants.
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Virtual eConsent improves accessibility and compliance in decentralized trials, streamlining enrollment with a secure, user-friendly process for informed consent in remote research.
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By advocating these three essential best practices, learn how stakeholders can navigate the complexities of eConsent adoption with confidence and enhance the overall efficiency and success of clinical trials.
EPRO RESOURCES
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See how a team of four managed data for 40 peer-reviewed studies and 200,000 participants.
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In honor of World Movement Disorders Day, we highlight advances in Parkinson’s disease care. At the 2024 MDS Congress, Signant presented research on electronic diaries for tracking PD patients' functional status.
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Access real-world examples of how electronic patient-reported outcome measures (PROMs) optimize data quality and reliability and improve the statistical power of trial data.