White Paper

Why eConsent Primes Patients And Studies For Success

Source: Medable
Medical data ipad iStock-1182616138

For almost 100 years, the informed consent process took place at a clinical trial site, with investigators briefing potential participants, in person, over large stacks of paper reminiscent of a car or housing loan. Thanks to technological innovations, refined processes, and decades of lessons learned, we have a better way of ensuring trial participants are educated and informed about their trial. This ”better way” is called eConsent, and it uses a combination of audio/visual presentation styles, proven educational techniques, and more to put the “informed” back into informed consent.

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