CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS
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Telehealth In Clinical Trials: What Sites And Patients Think
Sites 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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Pick The Right PV Technology With Help From A Safety Data Management Expert
Otsuka'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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Ensure alignment with your study protocol by leveraging the Sculptor portal to simulate eDiary completion and top-down scheduling, allowing for real-time preview and modifications.
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Learn why having a strong and robust eCOA solution, along with an understanding of the specific challenges of this therapeutic area, is critical to the success of immuno-inflammation clinical trials.
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Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
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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Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.
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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.
EPRO RESOURCES
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Dive into considerations when deciding on the best COAs to implement as well as best practices when developing your eCOA strategy in this blog.
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If you are in the early stages of an oncology trial, there is a lot to consider when it comes to your data management and how the process can be simplified by improving how your study captures data.
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Explore how consent is a critical step that can greatly influence patient enrollment, adherence and retention in the trial.