Is the availability of more advanced, integrated cloud-based platforms the panacea the industry so desperately needs to tackle the stagnation of clinical trial performance or is automation the precursive step towards more significant improvements in study execution?
This webinar explores how the right EDC system empowers you to conduct your research on your own terms - without relying on the schedule and workflow of external parties.
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.
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