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Unlocking the Potential of eConsent: Demystifying Electronic Signatures
eConsent is just an electronic version of the existing informed consent process, a process that in itself is often mistakenly viewed as the same as getting a participant’s signature on the consent form. In reality, the signature is only part of the process. The consent process itself comprises two elements…
The real value of eConsent in clinical trials
There is still a reluctance to adopt more innovative approaches among sponsors and clinical research organizations (CROs) because sometimes the clinical trial model just isn't compatible with those innovations and other times, they feel it is too complicated to introduce different technologies into clinical trials. Adding eSource into your clinical trial is one way to get started with decentralized technologies and the potential burdens are outweighed by the value…