How to proceed
If your dataset contains potentially sensitive data, please consult our Step-by-Step Guide on Data Publication for ETH Zurich Researchers. It contains information on the necessary steps to prepare your dataset for publication.
If your dataset contains health-related personal data, we additionally recommend consulting Scientific IT Services before publication.
Any disclosure risk must always be assessed at the level of the individual case. The ultimate responsibility for this lies with the researchers who submit a dataset for publication.
Which potentially sensitive data may be included in the Research Collection?
In addition, use the following table to check whether and under what conditions your dataset can be included in the Research Collection.
Due to legal, security and ethical requirements, the Research Collection is only suitable to a limited extent as a repository for publishing and archiving potentially sensitive data. The criteria in the following table must therefore be observed.
Data type | Can it be deposited in the Research Collection? | Examples |
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Health-related personal data covered by the Human Research Act. | No, if not anonymized and/or no consent for publication resp. archiving is given. No, provided it is information that directly identifies individuals (e.g. tables with keys used to de-identify a patient by coding / pseudonymization). Yes, provided irreversible anonymization and consent of data subjects for publication resp. archiving has been obtained. Please however note the following caveats and general conditions:
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Ohter highly sensitive personal data | No To determine whether your research data is highly sensitive personal data that must be classified as ‘strictly confidential’, you must perform a classification and risk assessment in accordance with the Directive "Inventarisierung und Klassifizierung von Informationen an der ETH Zürich" (Inventory and Classification of Information at ETH Zurich). |
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Personal research data that are not subject to the Human Research Act (cf. Art. 5 Data Protection Act) and have not been classified as highly sensitive (cf. above) | Yes, provided
| Not classified as highly sensitive or health-related
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Non-personal, strictly confidential research data | No To determine whether your research data is strictly confidential, you must carry out a classification and risk assessment in accordance with the Directive "Inventarisierung und Klassifizierung von Informationen an der ETH Zürich" (Inventory and Classification of Information at ETH Zurich). |
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Unpublished research data subject to export controls | No Information on classification can be found on the export control web pages. |
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Administrative documents | Usually no Such documents are generally not intended for publication or sharing with other researchers, so a public repository is not the most appropriate tool for preservation. We recommend that such documents be archived in an appropriate internal repository of the research group or department. | Data documenting administrative processes related to a research project, e.g.
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Further information
Literature
Gahl, Brigitta; Haynes, Alan G; Sluka, Constantin; et al. (2022). Sharing of Data from Clinical Research Projects. Guidance from the SCTO’s CTU Network. Published by the Swiss Clinical Trial Organisation (SCTO). https://doi.org/10.54920/SCTO.2021.02
Krügel, Sybil (2019). The informed consent as legal and ethical basis of research data production. FORS Guide No. 05, Version 1.0. Lausanne: Swiss Centre of Expertise in the Social Sciences FORS. https://doi.org/10.24449/FG-2019-00005
Puebla, Iratxe; Lowenberg, Daniella; FORCE11 Research Data Publishing Ethics WG. (2021). Joint FORCE11 & COPE Research Data Publishing Ethics Working Group Recommendations. Zenodo. https://doi.org/10.5281/zenodo.5391293
Laws and guidelines
Directive "Informationssicherheit an der ETH Zürich" dated 17 December 2024 (German)
Directive "Inventarisierung und Klassifizierung von Informationen an der ETH Zürich" dated 1 January 2025 (German)
Factsheet Data Protection in Research Projects of December 2019, Legal Services of ETH Zurich
Federal Act on Data Protection (FADP) of 25 September 2020 (Status as of 1 September 2023)
Federal Act on Research involving Human Beings (Human Research Act, HRA) of 30 September 2011 (Status as of 26 May 2021)
Ordinance on Human Research with the Exception of Clinical Trials (Human Research Ordinance, HRO) of 20 September 2013 (Status as of 26 May 2022)