We are gathering information regarding industry experience, perceptions, and expectations around the use of electronic informed consent (eConsent) in clinical trials. Your responses will help inform strategies for improving the use of this technology for the benefit of participant, sites, and sponsors.
The survey should take approximately 15-20 minutes to complete. Your responses are anonymous unless you chose, at the end, to provide your email for further involvement in this research or related initiatives from the European Forum for Good Clinical Practice.
EFGCP eConsent initiative is a non-profit multistakeholder initiative focusing on harmonizing terminologies and processes associated with eConsent, to increase insight in different stakeholder value models and to provide a consistent country-level overview of acceptance/non-acceptance of certain eConsent aspects. A common misunderstanding on eConsent is that it is about remote consenting or electronic signatures, however these are just some of the features that could be used for eConsent. A glossary of various eConsent digital features has been created by the EFGCP eConsent team and can be accessed here