You are invited to attend this FREE online event, hosted by the UK Trial Managers' Network, UKCRC Registered CTU Network and the MRC-NIHR Trials Methodology Research Partnership.
The event has been designed for clinical trialists to hear about and share best practice, ideas and challenges when implementing electronic consent methods into clinical trials.
For the purposes of this event, e-consent is defined as: "the use of any electronic media (such as text, graphics, audio, video, podcasts or websites) to convey information related to the study and to seek and/or document informed consent via an electronic device such as a smartphone, tablet or computer”, as per the MHRA definition.
The focus of this event will be on the TAKING and RECORDING of consent, by electronic means. We will not be covering the broader topic of 'information giving' during the informed consent process.
Event programme
13:00 - Welcome and introductions
13:10 - National e-consent survey results
13:25 - Case study presentation 1
13:30 - Case study presentation 2
13:35 - Case study presentation 3
13:35 - Questions with case study presenters
13:45 - Regulatory and governance aspects
13:55 - Discussion groups
14:40 - Break
14:50 - Feedback and discussion with panel
16:00 - Close
Please note, this programme is subject to change prior to the event.
This event will be hosted via MS Teams, and places are therefore limited. Places will be offered on a first come first served basis.
Please note, block booking of tickets for groups of people is not permitted. You may only book ONE individual ticket.
If you have any questions about this event, please email [email protected]
