Mind the gap with Europe. Why public interest cannot be a good reason to perform observational and epidemiological research?

Author:

Cagnazzo Celeste1ORCID,Ficara Bruno1,Palermo Federica2,Fagioli Franca1

Affiliation:

1. SC Oncoematologia Pediatrica – Ospedale Infantile Regina Margherita, AOU Città della Salute e della Scienza di Torino, Torino, Italy

2. SC SS Clinical Trial Center Fondazione, IRCCS Istituto Nazionale Tumori di Milano, Milan, Italy

Abstract

The consequences of the Italian privacy legislation, that represents a very restrictive implementation of the general European regulation on data protection, have mainly been felt at the level of observational research. In this field is not always possible to obtain the consent of subjects, and as for retrospective studies, it is not currently clear which is the correct regulatory procedure to follow. This uncertainty in the law’s implementation has given way to multiple interpretations, making it difficult to obtain a homogeneous path in Italy. However, it is possible that the observation point has been totally wrong so far and that it would be more correct to choose a different legal bases than consent, both to preserve scientific progress and collective ethics, without losing the protection of the subject. This approach, which has already been followed by other European countries, could bring us closer to the rest of Europe and allow us to competitively participate in community projects that we are often cut off from.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

Reference17 articles.

1. Senato della Repubblica Italiana. Costituzione Italiana, Art. 13 e 32, https://www.senato.it/node/14/printable/print (accessed 25 July 2023).

2. Presidente della Repubblica Italiana. LEGGE 28 marzo 2001; Ratifica ed esecuzione della Convenzione del Consiglio d'Europa per la protezione dei diritti dell'uomo e della dignita' dell'essere umano riguardo all'applicazione della biologia e della medicina: Convenzione sui diritti dell'uomo e sulla biomedicina, fatta a Oviedo il 4 aprile 1997, nonche' del Protocollo addizionale del 12 gennaio 1998, n. 168, sul divieto di clonazione di esseri umani, 2001. https://www.gazzettaufficiale.it/eli/id/2001/04/24/001G0201/sg (accessed 25 July 2023).

3. Centro di Coordinamento Nazionale del Comitati Etici. Linee di Indirizzo per la Raccolta del Consenso Infor-mato alla Partecipazione a Sperimentazioni Cliniche, 2020. https://www.aifa.gov.it/documents/20142/1619588/linee_indirizzo_centro_coordinamento_20_05_2022.pdf (accessed 25 July 2023).

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