IQVIA Complete Consent provides an easy, secure way to deliver highly engaging, regulatory compliant electronic consent for trials of all types.
Gain insight into why pharma companies generally seek IRT vendor relationships to ensure high-quality builds that meet their needs and avoid the potential pitfalls associated with RTSM.
Download this guide for five key recommendations on how to build an eCOA strategy in your next oncology trial that keeps your patient's voice front and center in their care.
In clinical trials, data capture is typically centered around patients’ experiences with a drug. Discover why electronic clinical outcome assessments (eCOAs) are essential to patient data capture.
Delve into how IQVIA eCOA captures patient data in a way that always keeps patients top of mind.
In this webinar, eCOA experts will explore how to implement a BYOD strategy, relevant BYOD regulatory considerations, and where the market is going from here.
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.
Dive into how the shift to patient reported outcomes has made Clinical Outcome Assessments (COAs) an increasingly necessary and often required tool in the clinical research landscape.
The value of eCOA tools is undisputed, but using a waterfall methodology of software delivery is highly inefficient. Explore how a more agile approach to eCOA development can produce a fully functional eCOA in a day.
Learn how an eCOA tool can provide patients a chance to be heard while giving sponsors quantitative and qualitative data to track the efficacy of a treatment.
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