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Updated: Apr 30, 2026

Perspectives on Neuroscience
Published on: July 31, 2007
Banking (on) the brain: from consent to authorisation and the transformative potential of solidarity
Shawn H E Harmon1, Aisling Mcmahon2
1School of Law, University of Edinburgh, Old College, South Bridge EH89YL, UK J Kenyon Mason Institute for Medicine, Life Sciences and Law, University of Edinburgh, South Bridge, UK shawn.harmon@ed.ac.uk.
Abstract:
Modern technologies and biomedicine ambitions have given rise to new models of medical research, including population biobanking. One example of biobanking is brain banking, which refers to the collection and storage of brain and spinal cord samples for research into neurological diseases. Obviously, brain banking involves taking brains and tissue from deceased people, a fact which complicates the role of recruiters and makes consent a poor tool for stakeholders. After contextualising brain banking and considering the public health issues at stake, this article explores the legal definitions and demands of, and actual processes around, consent in England/Wales/Northern Ireland and authorisation in Scotland, articulating and evaluating their conceptual and practical differences. It then argues for an expanded but improved operation of 'authorisation' in the brain banking (and broader biobanking) setting, adopting 'solidarity' as our foundation and the improvement of the 'public good' our objective.
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