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eConsent is rapidly becoming the new consent standard for trials. Due to COVID and a general need to simplify the consent and tracking process, more and more trials are using this solution. In our webinar, we will look into selecting the right eConsent solution to your study type and how to simplify the eSignature process for the patient.
Site benefits of eConsent are essential, and most sites find eConsent is easier to use and makes it easy to fulfil the regulatory requirements. We will go through the site process of using eConsent for both initial- and re-consent, and how this is linked to randomization and EDC.