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Maximizing Site Performance: The Hidden Benefits of Unified eConsent and EDC
Let’s be real: managing clinical trials is tough enough without juggling multiple disconnected systems. Yet for many research teams, that’s…
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eConsent: What it is and Why your eClinical Software Should Have it
Unsure of how eConsent should tie into your eClinical platform? This post explains just why electronic informed consent is an important component of your technology toolkit.
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Still Using Paper CRFs in Clinical Trials?
How does a fully remote trial look from start to finish? Our Chief Medical Officer, Dr. Leigh Mack, walks us through it step-by-step.
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Mobile Devices and Wearables: The New Source Document
In this post, CMO Dr. Leigh Mack explains how wearable devices and smartphones will play a major role in the consent process and in patient reported outcomes as clinical trials evolve.
