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What can data trusts for health research learn from participatory governance in biobanks?
Richard Milne
,
Annie Sorbie
,
Mary Dixon-Woods
OAI: oai:www.repository.cam.ac.uk:1810/319096
•
DOI: 10.17863/CAM.66212
Published by:
Abstract
general
Informed Consent
patient perspective
research ethics
scientific research
Biological Specimen Banks
Humans