Discover how the right eConsent tool will pay dividends by delivering real-world efficiency and improved compliance.
Is your research organization prepared to take advantage of innovative tools and technologies that are available for clinical research today?
Learn what it takes to bring all silos of information together for actionable insights.
During this webinar, informed consent experts with decades of hands-on monitoring experience discuss the challenges they’ve encountered and how to overcome them with the integration of eConsent.
In this video, Jery Grupp draws on his rich background with Merck and Janssen to explain how eCOA technology supports data integrity and validation.
Some clinical trials study pediatric populations, which requires the child or a parent / caregiver to complete a diary regarding the child's wellbeing. Is it possible or even regulator-accepted to perform pediatric clinical trials using eCOA? Dr. Jill Platko explains in this short video.
Learn how to enhance your ePRO functionality and your patient engagement efforts.
Some clinical trials study pediatric populations, which requires the child or a parent / caregiver to complete a diary regarding the child's well being. Is it possible or even regulator-accepted to perform pediatric clinical trials using eCOA? Dr. Jill Platko explains in this short video.
eConsent is the next technology to be adopted by clinical study teams, but many simply don't know where to begin when taking the next step. In this video, Sandra "SAM" Sather, gives her tips for implementing an eConsent solution.
Protect the safety of trials subjects and give medical monitors the ability to increase the quality and speed of their work with this solution.
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