Template for the SNSF Data Management Plan
prepared by
Please note
Recommendations on this page are intended to illustrate the guidelines and other information provided by the SNSF for preparing Data Management Plans. The SNSF’s guidelines are binding.
The creation of former versions of this page was mandated by swissuniversities as part of the DLCM project. The earlier versions of this page were prepared jointly by teams from the libraries of EPFL and ETH Zurich, with input from DLCM partners. The included content exists in adapted versions for the two universities. It can also be freely adapted to other institutions’ needs. The examples therefore do not cover all disciplines. Further examples from other subject areas as well as feedback or questions concerning ETH Zurich and other feedback are welcome to data-management@library.ethz.ch for possible inclusion in future revisions.
Version ETH Zurich 3
License Creative Commons CC BY-SA
Table of Contents
1. Data collection and documentation
2. Ethics, legal and security issues
3. Data storage and preservation
How to work with this template
A DMP for the SNSF must be entered in a webform on the mySNF-platform. This page will guide you through the process of collecting the necessary information and formulating the input. It compiles and relies on the binding guidelines from the SNSF, which have priority in any case of doubt.
The first version of your DMP can be considered as a draft. It can and must be adapted as the implementation of the project and its data management evolve.
Each section of this template contains:
- Section heading from SNSF
- Questions to consider
- Recommendations for completing the section
- Examples of inputs from different DMPs.
Please note: these examples should only give you an idea of how to state certain information. You are welcome to re-use parts of the examples for your own means. Nevertheless, the content must be adapted to the situation in your project. In addition, be aware that these examples do not always cover the entire section in question and need to be completed. - Contact information at ETH Zurich
SNSF Data Management Plan
Institution
ETH Zurich
Responsibilities
Principal Investigator:
(Specify name and email)
Data management plan contact person:
(Specify name and email)
1. Data collection and documentation
1.1 What data will you collect, observe, generate or re-use?
Questions you might want to consider
What type, format and volume of data will you collect, observe, generate or reuse?
Which existing data (yours or third-party) will you reuse?
Briefly describe the data you will collect, observe or generate. Also mention any existing data that will be (re)used. The descriptions should include the type, format and content of each dataset. Furthermore, provide an estimation of the volume of the generated datasets.
This relates to the FAIR Data Principles F2, I3, R1 & R1.2
Recommendations
For each dataset in your project (including data you might re-use) mention:
Data type: Briefly describe categories of datasets you plan to generate or use, and their role in the project
Data origin: to be mentioned if you are reusing existing data (yours or third-party one). Add the reference of the source if relevant.
Format of raw data (as created by the device used, by simulation or downloaded): open standard formats should be preferred, as they maximize reproducibility and reuse by others and in the future [see List of recommended file formats by ETH Zurich]
Format of curated data (if applicable): open standard formats should be preferred [see List of recommended file formats by ETH Zurich]
Estimation of volume of raw and curated data.
Examples of answer to be adapted to your research application
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
1.2 How will the data be collected, observed or generated?
Questions you might want to consider
What standards, methodologies or quality assurance processes will you use?
How will you organize your files and handle versioning?
Explain how the data will be collected, observed or generated. Describe how you plan to control and document the consistency and quality of the collected data: calibration processes, repeated measurements, data recording standards, usage of controlled vocabularies, data entry validation, data peer review, etc.
Discuss how the data management will be handled during the project, mentioning for example naming conventions, version control and folder structures.
This relates to the FAIR Data Principle R1
Recommendations
What standards, methodologies or quality assurance processes will you use?
For each dataset in your project (including data you might re-use) mention:
the use of core facility services (specify their certifications, if any),
whether you follow double blind procedures (define it),
the use of standards or internal procedures; describe them briefly.
If you are working with persons’ data, confirm the following:
have the subjects of your data collection (persons) been fully informed (what data do you collect, what will you do with the data, and who will receive it; when will they be deleted) and have the subjects given their informed consent?
- have the subjects of your data collection (persons) been informed about their rights on information, data deletion and data correction?
How will you organize your files and handle versioning?
Indicate and describe the tools you will use in the project.
You may rely on the following tools depending on your needs:
a naming convention, i.e. the structure of folders and file names you will use to organize your data.
For example: Project-Experiment-Scientist-YYYYMMDD-HHmm-Version.format (concretely: Atlantis-LakeMeasurements-Smith-20180113-0130-v3.csv)
a code revision management system, such as Git. Several Git servers are available for ETH domain: c4science.ch, gitlab.epfl.ch, gitlab.ethz.ch.
- a data management system, such as an Electronic Laboratory Notebook / Laboratory Information System (ELN/LIMS). Within ETH domain, examples of used ELN/LIMS: openBIS, SLims.
- Additional ETH Zurich services:
- The ETH Research Data Hub (ETH RDH) is an ETHZ-wide data management solution for quantitative research groups that provides the lowest entrance barrier for labs that do not need extensive customization.
- The ETH Research Data Node (ETH RDN) is a specific data management instance for one research lab and can be customized more extensively if needed.
Examples of answer to be adapted to your research application
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
Scientific IT Services: https://sis.id.ethz.ch/
1.3 What documentation and metadata will you provide with the data?
Questions you might want to consider
What information is required for users (computer or human) to read and interpret the data in the future?
How will you generate this documentation?
What community standards (if any) will be used to annotate the (meta)data?
Describe all types of documentation (README files, metadata, etc.) you will provide to help secondary users to understand and reuse your data. Metadata should at least include basic details allowing other users (computer or human) to find the data. This includes at least a name and a persistent identifier for each file, the name of the person who collected or contributed to the data, the date of collection and the conditions to access the data.
Furthermore, the documentation may include details on the methodology used, information about the performed processing and analytical steps, variable definitions, data dictionary, codebook, references to vocabularies used, as well as units of measurement.
Wherever possible, the documentation should follow existing community standards and guidelines. Explain how you will prepare and share this information.
This relates to the FAIR Data Principles I1, I2, I3, R1, R1.2 & R1.3
Recommendations
Indicate all the information required to be able to read and interpret the data (context of data) in the future. General documentation of the data is often compiled into a plain text or markdown README file. These formats may be opened by any text editor and are future-proof.
In addition, for each data type
Provide the metadata standard used to describe the data (for concrete examples see: https://fairsharing.org/standards/, https://bartoc.org, or Research Data Alliance Metadata Standards Directory). If no appropriate (discipline oriented) existing standard is available, you may describe the ad hoc metadata format you will use in this section. Metadata 1 may also be embedded in the data (e.g. embedded comments for code). Or, when for example using Hierarchical Data Format HDF5, arbitrary machine readable metadata can be included directly at any level.
Describe:
the software (including its Version) used to produce the data and the software used to read it (they can be different)
the format and corresponding filename extension and its version (if possible).
The used software should be archived along with the data (if possible, depending on the software license).
Describe the automatically generated metadata, if any.
Provide the data analysis or result together with the raw data, if possible.
Additional information that are helpful in a README file
description of the used software,
description of the used system environment,
description of relevant parameters such as:
geographic locations involved (if applicable)
all relevant information regarding production of data.
1 Metadata refers to “data about data”, i.e., it is the information that describes the data that is being published with sufficient context or instructions to be intelligible for other users. Metadata must allow a proper organization, search and access to the generated information and can be used to identify and locate the data via a web browser or web based catalogue.
Examples of answer to be adapted to your research application
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
Scientific IT Services: https://sis.id.ethz.ch/
2. Ethics, legal and security issues
2.1 How will ethical issues be addressed and handled?
Questions you might want to consider
- What is the relevant protection standard for your data? Are you bound by a confidentiality agreement?
- Do you have the necessary permission to obtain, process, preserve and share the data? Have the people whose data you are using been informed or did they give their consent?
- What methods will you use to ensure the protection of personal or other sensitive data?
Ethical issues in research projects demand for an adaptation of research data management practices, e.g. how data is stored, who can access/reuse the data and how long the data is stored. Methods to manage ethical concerns may include: anonymization of data; gaining approval by ethics committees; formal consent agreements. You should outline that all ethical issues in your project have been identified, including the corresponding measures in data management. In case not all ethical issues of your research project are solved yet, you might check for additional information or resources on the ETHics Resource Platform (https://www.ethicsrp.ethz.ch/).
If you assess that there are no ethical issues in your project, you can use the following statement: There are no ethical issues in the generation of results from this project.
This relates to the FAIR Data Principle A1
Recommendations
Description and management of ethical issues
Describe which ethical issues are involved in the research project (for example, human participants, collection/use of biological material, privacy issues (confidential/sensitive data), animal experiments, dual use technology, etc.).
For more information, see
- ETH Zurich Guidelines on scientific integrity, RSETHZ 414 (as of 01.01.2022)
- The ETH Zurich Compliance Guide
Explain how these ethical issues will be managed, for example:
The necessary ethical authorizations will be obtained from the competent ethics committee.
Informed consent procedures will be put in place.
Personal/sensitive data will be anonymized.
Access to personal/sensitive data will be restricted.
Personal/data will be stored in a secure and protected place.
Protective measures will be taken with regard to the transfer of data and sharing of data between partners.
Sensitive data is not stored in cloud services (e.g. data related to individuals, data under a non-disclosure agreement, data injuring third party rights or (legal) expertises).
Please check if your project involves data relating to (in bold) one of the following ethical issues:
- Human participants (This includes all kinds of human participation, incl. non-medical research, e.g. surveys, observations, tracking the location of people)
- Human cells/tissues
- Human embryonic stem cells
- A clinical trial
- The collection of personal/sensitive/confidential data
- Animal experimentation
- Developing countries (access and benefit sharing)
- Environmental and/or health and safety issues (for example, a negative impact on the environment and/or on the health and safety of the researchers.)
- The potential for military applications (dual-use technology).
Ethical authorizations
If your project involves human subjects, an ethical authorization from either the cantonal ethics commission or the institutional ethics commission (ETH Zurich Ethics Commission) is needed. This depends on whether your project is invasive/non-invasive and whether or not health-related data is collected/used.
For research involving work with human cells/tissues, a description of the types of cells/tissues used in their project needs to be provided, together with copies of the accreditation for using, processing or collecting the human cells or tissues.
Research which involves the collection or use of personal data needs to be reviewed by the cantonal ethics commission or the ETH Zurich Ethics Commission’s (depending on what kind of data is involved). ETH Zurich: For more information, see the ETH Zurich Ethics Commission’s website (German).
If animal experiments are conducted in the context of the research project, an authorization of the cantonal veterinarian office is needed.
(See also: ETH Zurich Animal Welfare Officer)- Dual-Use technologies (civil and military purposes): Transfer of knowledge, software, demonstrators or prototypes could fall under the scope of the Swiss Goods Control Act (GCA) and its Ordinance (GCO) in the context of technology transfer or research proposals, but also informal personal contacts. In case any US-technology is involved in research, the US-export control regulations should not be disregarded. Before transmission of information, research results, prototypes etc. to a company, person or institution (even academic) outside of Switzerland, it must be checked whether the data/information or material to be transmitted is subject to authorization
For more information, see the ETH Zurich Export Control website.
- Research that may have a negative impact on the environment, for example research with Genetically Modified Organisms (GMO), requires an authorization from the Federal Office for the Environment (FOEN). If the research project has a negative impact on the health and safety of the researchers involved (for example if the research proposal involves the use of elements that may cause harm to humans), authorizations for the processing or possession of harmful materials must be requested.
More information can be obtained from the ETH Zurich Safety, Security, Health, Environment department (SSHE / SGU).
Examples of answer to be adapted to your research application
References
ETH Zurich Guidelines on scientific integrity, RSETHZ 414 (as of 01.01.2022)
Guidelines for Research Data Management at ETH Zurich, RSETHZ414.2 (as of 01.07.2022)
The ETH Zurich Compliance Guide
Federal Data Protection and Information Commissioner
Contact for assistance – ETH Zurich
Ethics Commission (Website or Contact: raffael.iturrizaga@sl.ethz.ch)
Website of Legal Office (e.g. for Data Protection issues)
Website of the Animal Welfare Officer (status 04.11.2022)
Website of Safety, Security, Health, Environment department (SSHE / SGU)
2.2 How will data access and security be managed?
Questions you might want to consider
What are the main concerns regarding data security, what are the levels of risk and what measures are in place to handle security risks?
How will you regulate data access rights/permissions to ensure the security of the data?
How will personal or other sensitive data be handled to ensure safe data storage and transfer?
If you work with personal data or other sensitive data, you should outline the security measures in order to protect the data. Please list formal standards which will be adopted in your study. An example is ISO 27001-Information security management. Furthermore, describe the main processes or facilities for storage and processing of personal or other sensitive data. (This relates to the FAIR Data Principle A1.)
Recommendations
The main concerns regarding data security are data availability, integrity and confidentiality, in particular the levels of risks involved and technical and organizational measures as named in the Swiss Federal Act on Data Protection.
The main concerns regarding data security are data availability, integrity and confidentiality.
Define whether :
- the level of the data availability risk is : low/medium/high.
- the level of data integrity risk is : low/medium/high.
- the level of data confidentiality is : low/medium/high.
You may choose some of the following options :
Regarding anonymization / encryption:
- All personal data will be anonymized in such a way that it will be impossible to attribute data to specific persons.
- All personal data will be pseudonymized. The correspondence table will be encrypted and access restricted to the project leader.
- All sensitive data will be encrypted and encryption keys will be managed only by authorized employees.
- Sensitive data transfers will be end-to-end encrypted.
Regarding access rights:
- Sensitive data will be accessible only by authorized participants to the project. The list of authorized participants will be managed by…
- Data access rules will be detailed in before starting the project.
- Access to the data/database will be logged, thus each access is traceable.
- Access to laboratory and offices will be restricted to authorized persons. The list of authorized persons will be managed by…
Regarding storage and back-up:
- All data will be backed-up on a regular basis and access to backup media will be managed according to data access rules. Backups will be stored in another location.
- All damaged media containing sensitive data will be physically destroyed.
- All servers will be located in a datacentre with restricted access. The datacentre is based in [country] (preferably data are stored at ETH Zurich).
- No data will be stored on a public cloud / cloud hosted outside Switzerland.
- No sensitive/personal data will be stored in cloud service external to ETH Zurich. “Sensitive data can be for example data related to individuals, data under a non-disclosure agreement, data injuring third-parties rights or legal expertise).
- All computers storing or computing sensitive data will not be connected to the Internet.
- All computers storing or computing sensitive data will have a hardened configuration (disk encryption, restricted access to privileged accounts to a small, controlled group of users, restricted or disabled remote access using privileged accounts, disabled guest or default accounts, local firewall, automatic screen lock with password protection, disabled remote out-of-band management (IPMI, Active Management Technology (AMT), etc.), disabled USB ports, removable privacy filter on screens, automatic updates via “Windows Update”, Apple’s “Software Update” or Linux “yum auto-update”, anti-virus software, Adobe’s “Flashplayer” and “Java” runtime).
Please note
In May 2018, the EU General Data Protection Regulation (GDPR, Regulation (EU) 2016/679) has come into force. This influences future cooperation with any EU-based partners and will be implemented in Swiss law, as well.
GDPR introduces an approach of “Privacy by Design” for parties working with personal or other sensitive data, requiring projects to define their data protection measures from the beginning.
Where the GDPR applies you must outline in a Data Protection Impact Analysis (DPIA, text or table, see an example of the ICRC) the risks involved to the rights of your studies’ subjects and the security measures foreseen in order to protect the data. This is crucial for your project. The less risks you have, the better. The more data safeguards you can imply, the better. The earlier stage you imply them at, the better.
(Cf. Art 35 of the EU General Data Protection Regulation entering into force May 2018)
Examples of answer to be adapted to your research application
References
ETH Zurich Guidelines on scientific integrity, RSETHZ 414 (as of 01.01.2022)
Guidelines for Research Data Management at ETH Zurich, RSETHZ414.2 (as of 01.07.2022)
The ETH Zurich Compliance Guide
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
Website of the Legal Office (e.g. for Data Protection issues)
IT Support Groups in the Departments
Website of the Scientific IT Services
2.3 How will you handle copyright and Intellectual Property Rights issues?
Questions you might want to consider
Who will be the owner of the data?
Which licenses will be applied to the data?
What restrictions apply to the reuse of third-party data?
Outline the owners of the copyright and Intellectual Property Right (IPR) of all data that will be collected and generated including the licence(s). For consortia, an IPR ownership agreement might be necessary. You should comply with relevant funder, institutional, departmental or group policies on copyright or IPR. Furthermore, clarify what permissions are required should third-party data be re-used.
This relates to the FAIR Data Principles I3 & R1.1
Recommendations
Attaching a clear license to a publicly accessible data set allows other to know what can legally be done with its content. When copyright is applicable, Creative Commons licenses are recommended. However, Creative Commons licenses are not recommended for software.
Amongst all Creative Commons licenses, CC0 “no copyright reserved” is recommended for scientific data, as it allows other researchers to build new knowledge on top of a data set without restriction. It specifically allows aggregation of several data sets for secondary analysis. Several data repositories impose the CC0 license to facilitate reuse of their content.
In order to enable a data set to get cited, and therefore get recognition for its release, it is recommended to attach a CC-BY “Attribution” license to the record, usually a description of the dataset (metadata). To get recognition, data sets can be cited directly. However, to increase their visibility and reusability, it is recommended to describe them in a separated document licensed under CC BY “Attribution”, such as a data paper or on the institutional repository.
When the data has the potential to be used as such for commercial purposes, and that you intend to do so, the license CC BY-NC allows you to keep the exclusive commercial use.
Reuse of third-party data may be restricted. If authorised, the data must be shared according to the third party’s original requirement or license.
For licensing of software at ETH Zurich, please see https://documentation.library.ethz.ch/pages/viewpage.action?pageId=9208031
Examples of answer to be adapted to your research application
References
ETH Zurich Guidelines on scientific integrity, RSETHZ 414 (as of 01.01.2022)
Guidelines for Research Data Management at ETH Zurich, RSETHZ414.2 (as of 01.07.2022)
The ETH Zurich Compliance Guide
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
Website of ETH transfer (e.g. for research contracts)
3. Data storage and preservation
3.1 How will your data be stored and backed-up during the research?
Questions you might want to consider
What is your storage capacity and where will the data be stored?
What are the back-up procedures?
Please mention what the needs are in terms of data storage and where the data will be stored.
Please consider that data storage on laptops or hard drives, for example, is risky. Storage through IT teams is safer. If external services are asked for, it is important that this does not conflict with the policy of each entity involved in the project, especially concerning the issue of sensitive data.
Please specify your back-up procedure (frequency of updates, responsibilities, automatic/manual process, security measures, etc.)
Recommendations
Institutional storage solutions:
For ETH Zurich, see storage options here and consult the IT Support Group of your Department.
Examples of answer to be adapted to your research application
Contact for assistance
Digital Curation Office: data-management@library.ethz.ch
Website of the Scientific IT Services
3.2 What is your data preservation plan?
Questions you might want to consider
What procedures would be used to select data to be preserved?
What file formats will be used for preservation?
Please specify which data will be retained, shared and archived after the completion of the project and the corresponding data selection procedure (e.g. long-term value, potential value for re-use, obligations to destroy some data, etc.). Please outline a long-term preservation plan for the datasets beyond the lifetime of the project.
In particular, comment on the choice of file formats and the use of community standards.
Recommendations
Describe the procedure, (appraisal methods, selection criteria …) used to select data to be preserved. Note that preservation does not necessarily mean publication (e.g. personal sensitive data may be preserved but never published), but publication means generally preservation.
This section should answer the following questions:
What data will be preserved in the long term - selection criteria, in particular:
Reusability of the data: quality of metadata, integrity and accessibility of data, license allowing reuse, readability of data (chosen file formats),
Value of the data: indispensable data, completeness of the data or data set, uniqueness, possibility to reproduce the data in the same conditions and at what cost, interest of the data, potential of reuse
Ethical considerations
Stakeholders requirements
Costs: additional costs that come for depositing data in a repository or data archive of your choice (costs anticipation and budgeting)
Selection basically has to be done together with or by the data producer or someone else with deep specialist knowledge.
What data curation process(es) will be applied, i.e.: anonymization (if necessary), metadata improvement, format migration, integrity check, measures to ensure accessibility.
Data retention period (0, 5, 10, 20 years or unlimited)
Decision to make the data public
Use of sensitive data (i.e. privacy issues, ethics, or intellectual property laws)
Definition of the responsible person for data (during the process of selection and after the end of the project)
For more information on useful criteria, see also Beagrie, Neil (2019). What to Keep: A Jisc research data study. Joint Information Systems Committee (JISC). Available at: https://repository.jisc.ac.uk/7262/1/JR0100_WHAT_RESEARCH_DATA_TO_KEEP_FEB2019_v5_WEB.pdf
In addition, select appropriated preservation formats (see section 1.1) and data description or metadata (see section 1.3).
Examples of answer to be adapted to your research application
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
IT Support Groups in the Departments
4. Data sharing and reuse
4.1 How and where will the data be shared?
Questions you might want to consider
On which repository do you plan to share your data?
How will potential users find out about your data?
Consider how and on which repository the data will be made available. The methods applied to data sharing will depend on several factors such as the type, size, complexity and sensitivity of data.
Please also consider how the reuse of your data will be valued and acknowledged by other researchers.
This relates to the FAIR Data Principles F1, F3, F4, A1, A1.1, A1.2 & A2
Recommendations
It is recommended to publish data in well established (or even certified) domain specific repositories, if available:
- A list of repositories recommended by the SNSF can be found on its webpage.
- re3data is a repository directory allowing to select repositories by subject and level of trust (e.g. certifications)
- ETH Zurich researchers are encouraged to publish data in ETH’s own Research Collection repository to ensure full compliance with ETH regulations.
In domains for which no suitable subject repositories are available, generalist repositories are available.
Among the most common used:
Zenodo (free, maximum 50GB/dataset, hosted by CERN)
Dryad (120$ for the first 20GB and 50$ for additional GB, Non-profit organization)
Figshare (free upload, maximum 5GB / dataset, commercial company)
Note
SNSF does not pay for storage in commercial data repositories (even though data preparation costs are eligible). Check the SNSF’s criteria for non-commercial repositories here (section 5.2). If you choose a commercial repository, read carefully the Terms of service to check if they respond to your needs and to your institutions’ ones as well as to your institutional (data) policy.
In order to make your data findable by other users, it is important that
each data packet and publication has a DOI (or similar persistent identifier) assigned,
they are deposited Open Access in a repository harvested by the main data services (e.g.: OpenAire, EUDAT,…).
Examples of answer to be adapted to your research application
References
SNSF’s criteria for non-commercial respositories
Contact for assistance – ETH Zurich
Digital Curation Office: data-management@library.ethz.ch
Website of the Research Collection
4.2 Are there any necessary limitations to protect sensitive data?
Questions you might want to consider
Under which conditions will the data be made available (timing of data release, reason for delay if applicable)?
Data have to be shared as soon as possible, but at the latest at the time of publication of the respective scientific output.
Restrictions may be only due to legal, ethical, copyright, confidentiality or other clauses. Describe your restrictions for data sharing due to ethical or legal constraints, preparation for patent application, security constraints, contractual obligations, intended commercial purposes and copyright issues as outlined in the Guidelines for Research Data Management at ETH Zurich. Be aware that confidential and/or person-related research data (as defined in footnote 4) can only be published in completely anonymised 9 form and in line with consent obtained from study participants. This purpose should already be considered when preparing consent forms for study participants.
Sensitive or confidential data are usually information relating to an identifiable person. Data can also be confidential, e.g., because they have to be protected from third-party access due to contractual agreements. If such data are used in a research project, the data management practice has to be adapted to deal with sensitive or confidential data in an appropriate way. Sensitive data are data that might cause serious harm when they fall into the hands of unauthorized persons. Regarding research data, sensitive data include but are not limited to sensitive personal data, research plans, contract agreements or geolocation data. Sensitive data must usually be classified as CONFIDENTIAL or STRICTLY CONFIDENTIAL[i] at ETH Zurich.
In case of business interests or similar restrictions, consider whether a non-disclosure agreement would give sufficient protection for confidential data.
This relates to the FAIR Data Principles A1 & R1.1
[i] Directive on “Information Security at ETH Zurich (RSETHZ 203.25) https://rechtssammlung.sp.ethz.ch/Dokumente/203.25en.pdf (as of 1 August 2021)
Recommendations
You may mention specifically the conditions under which the data will be made available:
there are no sensitive data
the data are not available at the time of publication
the data are not available before publication
the data are available after the embargo of …
the data are not available because of the patent of … for a period of…
Examples of answer to be adapted to your research application
References
ETH Zurich Guidelines on scientific integrity, RSETHZ 414 (as of 01.01.2022)
Guidelines for Research Data Management at ETH Zurich, RSETHZ414.2 (as of 01.07.2022)
The ETH Zurich Compliance Guide
Contact for assistance – ETH Zurich
Digital Curation office: data-management@library.ethz.ch
Ethics Commission (Website or Contact: ethics@sl.ethz.ch)
4.3 All digital repositories I will choose are conform to the FAIR Data Principles
[CHECK BOX]
Recommendations
The SNSF requires that repositories used for data sharing are conformed to the FAIR Data Principles. For more information, please refer to the SNSF’s explanation of the FAIR Data Principles.
You can find certified repositories in Re3data.org, an exhaustive registry of data repositories.
ETH Zurich’s Research Collection also complies with the FAIR Principles.
4.4 I will choose digital repositories maintained by a non-profit organisation
[RADIO BUTTON yes/no]
Recommendations
If you do not choose a repository maintained by a non-profit organization, you have to provide reasons for that.
One possible reason would be to ensure the visibility of your research, for example, if your research community is standardly publishing data on a well-established but commercial digital repository.
Please note that the SNSF supports only the use of non-commercial repositories for data sharing. Costs related to data upload are only covered for non-commercial repositories. Check the SNSF’s criteria for non-commercial repositories (section 5.2).
External useful resources
Digital Curation Centre glossary (alternatively, glossary in this Wiki: Glossary - Research Data Management)
List of useful tools prepared by the Swiss DLCM project