The scope of clinical trial tools has expanded rapidly over the last several years, with solutions such as eConsent, eCOA/ePRO, EDC and RTSM now becoming a normal part of the R&D toolkit. In fact, the market has surged with startups eager to capitalize on this continuing trend.
However, as companies approach what seems like so many options, it can seem incredibly overwhelming. What—if any—solutions do you actually need?
In this playbook, we speak with Melissa Newara, senior director of Subject Matter Expertise at Medrio, to explore what leaders should know as they compare eClinical technologies to generate high-quality data and achieve more efficient and optimized clinical studies. The playbook highlights:
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