On the other hand, eICs also raise privacy and secure data storage regulation compliance concerns. The eIC, if properly implemented, will be of significant benefit to institutional review boards (IRBs ...
Informed consent means making sure prospective participants understand what they are agreeing to before they choose whether ...
The Department of Health and Human Services’ (HHS) Office for Human Research Protections (OHRP) and the US Food and Drug Administration (FDA) on Wednesday finalized a question and answer (Q&A) ...
In today’s digital world, we often desire to have people consent to documents by merely pasting an image of a signature into a document, clicking a virtual button on a web site or mobile phone, or ...
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Electronic consent demonstrates potential to overcome 'key barrier' in stroke trial recruitment
Post-hoc analyses of a large, randomized clinical trial have revealed the potential advantages associated with electronic informed consent (eConsent) in acute ischemic stroke studies, including ...
Upon receiving information, patients were able to give preliminary consent on a survey form, and this allowed collection of a first blood sample and further communication. The use of an asynchronous ...
To determine the individual and combined effects of a simplified form and a review/retest intervention on biobanking consent comprehension. We conducted a national online survey in which participants ...
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