Abstract
Gaps in regulations pertaining to the collection and storage of biological materials in a biobank, at least in the European context, have made the writing of local guidelines essential from an ethical point of view. Nevertheless, until recently, the elaboration of local guidelines for the collection, use and storage of biological materials in a biobank has been the exception in Italy and all European countries. In this context, it is of value to know the policies, even if they are unwritten, of local ethics committees (ECs) engaged in the evaluation of research protocols involving biobanks and biological materials. This paper presents the results of a survey carried out among local Italian ECs (229) to document their attitudes and policies regarding the management of the ethical issues related to biobanks and the use of biological materials. A questionnaire was developed to investigate the areas regarded as critical from an ethical–legal point of view: informed consent and information to the subjects; protection of confidentiality; communication of research results; access/transfer of biological materials and related data; ownership of samples and data and intellectual property rights; and subjects’ remuneration and benefit sharing. Twenty-six ECs from the Italian Institutes for Research and Care (62%) and 26 other ECs (14%) participated in the survey.
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Acknowledgements
The work was conducted within the project FIRB 2006, ‘Bioethics and legal aspects in connection with biomedical research for processing, storage and use of human biological samples’ which was funded by the Italian Ministry of University and Research. During part of the project, CP was an academic visitor at the Ethox Centre, Oxford, UK, directed by Michael Parker.
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Porteri, C., Togni, E. & Pasqualetti, P. The policies of ethics committees in the management of biobanks used for research: an Italian survey. Eur J Hum Genet 22, 260–265 (2014). https://doi.org/10.1038/ejhg.2013.107
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DOI: https://doi.org/10.1038/ejhg.2013.107
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