Preparing For eConsent - A Step By Step Guide For Site Personnel

By Sam Sather, Regulatory & Quality, TrialConsent™, CRF Health

Electronic informed consent, or eConsent, is one technological advancement introduced to clinical trials that is escalating in its adoption. This blog highlights findings from a recent survey which sought to understand the impact of the consent process in clinical trials. The result: sites are interested in the development of eConsent…Read on to learn more about the survey and Sam Sather’s top tips for site personnel on developing an eConsent process.