Adequate and ethical informed consent for trials and other types of clinical research remains problematic. How to offer enough information without overwhelming, provide options for potential re-use of retained data and samples, and handle particularly complex trial designs or where consent-based challenges contribute to the exclusion of certain populations? The Global Health and Trial Conduct Working Groups will co-host a webinar showcasing perspectives on these issues from the UK, South Africa and Australia, which may also foster future innovation and collaboration.

This TMRP webinar will be presented by The Global Health and Trial Conduct Working Groups on behalf of The Global Health Network.

Register here.

Please note, you need to register for this event in order to receive an email invitation to join the session. Registrations are limited to 250 attendees and places will be offered on a first come first served basis.

This webinar will be hosted via MS Teams. You will need access to the web and sound facilities in order to view the webinar.

A recording of the webinar will be made available after the event. Previous recordings can be found here:
UKTMN members also have access to recordings via the UKTMN YouTube channel. 

If you have any questions regarding this event or wish to cancel your place, please email [email protected]

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