An EU multistakeholder forum has developed a new tool to support the uptake of eConsent in clinical trials and has provided guidance on how sponsors and other parties can tailor eConsent models appropriate for their specific studies, since a one-size-fits all approach does not exist.
Key Takeaways
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Despite clear advantage of eConsent over the paper-based informed consent process, the adoption of the electronic approach remains limited.
The “eConsent Fit-for-Purpose Study Framework” was published by the not-for-profit European Forum for Good Clinical Practice (EFGCP) on 12...
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