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eConsent with CRFWEB
Whether it’s to take advantage of the move towards decentralised clinical trials, to facilitate patient reported outcomes or simply to speed up patient recruitment and increase engagement, eConsent is an ever more critical tool in the clinical trial management process.
Like all our modules, eConsent is seamlessly integrated into the CRFWEB application. Subject data can be captured instantly online or offline and synced when a secure connection is available.
eConsent Features
Options for eSignature include:
- fingerprint recognition
- signature touchscreen collection
- subject video
- geo-location and timestamp
Options to enhance engagement include the facility to add content including:
- images, videos, questionnaires.
CRFWEB eConsent makes appropriate checks to ensure consent is provided before any study data is collected. The result is a compliant and secure process to enable subject sign up and help improve both sign up and retention rates.
