This webinar on electronic Informed Consent (eConsent) addresses the practical considerations when implementing eConsent. This topic has become an ever increasingly important topic as remote strategies and decentralised clinical trials are being deployed. The session starts with an introduction to the eConsent Implementation Practical Guide, which was published earlier this year. The Guide was developed by EUCROF and eClinical Forum members and addresses key themes and hot topics and provides a view on the modernisation of the clinical trials informed consenting process, including the current perception and shift of eConsent adoption in light of the COVID-19 pandemic.