(1) This Procedure is effective from 25 July 2024. (2) This Procedure outlines the requirements for responsible management of research data and information (data) in compliance with the Australian Code for the Responsible Conduct of Research, 2018 (the Code). (3) This Procedure applies to all research undertaken by staff and students of Deakin University irrespective of the location of the research. (4) This Procedure is pursuant to the Research Conduct Policy. (5) The University is responsible for: (6) Researchers are responsible for: (7) Researchers are strongly encouraged to use the University’s Research Data Management Planner, which details all the information required by this Procedure. (8) Each dataset must be assigned a data custodian who should be identified in the Plan. The custodian may be an individual or outside agency or an intermediary that manages data coming from a number of sources. (9) Where the data custodian is external to Deakin, a Deakin staff member should be appointed to act as a dual custodian to ensure custodial requirements are met. They will manage the data if the external custodian cannot. (10) The data custodian or Deakin dual custodian is responsible for: (11) The University is responsible for providing facilities that comply with: (12) Data relating to University research projects should be stored in the facilities, infrastructure and platforms provided and supported by the University. (13) Where data must be stored at a location outside the University, such as a public archive or for collaborative projects: (14) Data collected off campus must be stored securely and regularly transferred or transported to the University where relevant, including: (15) Data transfer must comply with any legislative requirements associated with the export or import of the research data out of or into Australia, or cross border transfer/transportation of the data, prior to the transfer or transportation of the data. (16) Where research data are collected online, researchers must take reasonable steps to ensure that the collection is legal in the data’s country or region of origin. (17) Data storage protocols must facilitate long-term preservation and retrieval of the data according to the University’s requirements. (18) Researchers will take all reasonable steps to ensure that research data subject to legislative or security requirements are managed appropriately to mitigate any risks to the University, the research team and any human participants involved in the research. Researchers will also take all reasonable steps to ensure that such data are not vulnerable to unauthorised access and stored securely. (19) Access arrangements may be restricted, shared or open and should be appropriate for the nature of the data, taking into account any relevant sensitivities or risks associated with sharing the data and complying with the relevant requirements of any associated ethics or biosafety approval processes. (20) Researchers must include a descriptive metadata record of their data that meets the University’s requirements and is stored in the University’s repository. (21) Ownership of research data will be determined by any of the following (where applicable): (22) Researchers should collect and store research data in such a way that it can be used in future research projects, unless there are valid reasons for not making data accessible, such as respect for cultural ownership or unmanageable risks to the privacy of research participants. (23) Restrictions to or proposed sharing or reuse of the research data and how the custodian will mediate access to the data (where applicable) should be included in the Plan. Reasonable efforts must be made to seek agreement from all relevant members of the research team prior to sharing or reusing the data. (24) The custodian must ensure a written agreement is in place prior to any sharing of data outside the research team, including any limitations to further sharing of the research data. (25) Reuse or sharing of human research data must comply with the human research ethics requirements, including ensuring future use of the data complies with any conditions of participant consent, or has been granted a waiver of the requirement for consent. (26) Where human biospecimens, non-human specimens or imported materials are shared, a copy of any relevant records relating to the management of the specimens must accompany the specimens. (27) Researchers must retain their data for the relevant period specified in the Research Data Retention Table at clause 40. (28) The relevant retention period for research data and the date data can be destroyed (if applicable) should be specified in the Plan and reviewed as appropriate. (29) Research data may be destroyed when it has reached the end of its applicable retention period and following consultation with the University Records Team. (30) Research data should be destroyed securely by one of the processes recommended on the University’s Research Data Management webpage. (31) Details of data destruction should be recorded in an existing register or the Plan by the data custodian. (32) Prior to leaving the University, researchers must provide access to the Plan and any physical or digital storage location/s with their direct line manager or supervisor. (33) Where the Deakin data custodian leaves the University, a new custodian must be appointed. Where the final member of a research team leaves the University, the Head of Academic Unit will take on the responsibilities of the data custodian unless other arrangements are made. (34) Researchers may take a copy of the research data for future use if they ensure that: (35) Deakin researchers conducting collaborative research across institutions must ensure that they comply with this Procedure. (36) Researchers should discuss and agree on a Data Management Plan and its requirements with collaborators, in writing, before conducting collaborative research across institutions. (37) Where applicable, a materials transfer agreement should be in place for material obtained from external institutions. (38) Researchers who have concerns regarding data management practices may seek confidential advice from Research Integrity Advisers regarding their obligations and options. (39) Potential breaches of the Code related to the management of data and information in research will be managed according to the Research Integrity Breaches Procedure. (40) The retention period specified in the following Data Retention Table commences (unless Exceptions* apply) when: (41) For the purpose of this Procedure:Research Data Management Procedure
Section 1 - Preamble
Section 2 - Purpose
Section 3 - Scope
Section 4 - Policy
Section 5 - Procedure
Data custodianship
Data storage and transfer
Data safety and security
Data access
Data description
Data ownership
Data reuse and sharing
Data retention
Data destruction
Researchers leaving the University
Collaborative research across institutions
Research Integrity Advisers (RIAs)
Breaches of the Code
Section 6 - Data Retention Table
Data type
Minimum retention period
ADMINISTRATIVE RESEARCH RECORDS AND RESULTS OF EXPERIMENTS
Records relating to the management and administration of specific individual research projects. Includes the development of research methodologies and protocols, resourcing, development and reporting on ethics applications, results of experiments, progress reporting to internal or external bodies and arrangements for informal collaborative research links with outside organisations. 7 years
RESEARCH DATA MANAGEMENT PLAN
Summary record of data created as part of research activities within the institution. Includes information about the nature and type of data, principal researchers or investigators, how long the data is to be retained, location and format of data and any conditions around access or reuse of the data. Permanent
DATA WITH THE FOLLOWING STIPULATED REGULATORY OR COMMUNITY SIGNIFICANCE
Data and datasets created as part of research activities within the institution, which are of regulatory or community significance. Includes data created that is:
- controversial or of high public interest;
- costly or impossible to reproduce;
- relates to the use of an innovative technique for the first time;
- of significant community or heritage value to the state or nation; or
- required by funding or other agreements to be retained permanently. Permanent
DATA FROM CLINICAL TRIALS
Data and datasets created from clinical trials as part of research activities within the institution. Excludes data and datasets with the regulatory or community significance stipulated above. 15 years
DATA FROM RESEARCH INVOLVING MINORS
Data and datasets created as part of research activities within the institution that involve minors. Excludes data and datasets with the regulatory or community significance stipulated above. 15 years after child reaches the age of 18
ALL OTHER TYPES OF RESEARCH DATA
Data and datasets created as part of research activities within the institution. Does NOT include data created for the specific research activities for which the additional regulatory requirements listed above apply. 5 years
Records relating to the management and administration of specimens obtained from humans for research purposes. Includes records documenting the use of human cadavers and body parts and all biospecimens including (but not limited to) tissue, blood, genes and organs.
Includes acquisition records, records relating to a specimen's condition and use in research projects, interventions undertaken on the specimen and destruction of the specimen or transfer and removal from the institution. Also includes records of the consent obtained from the participant for the use of their biospecimens including duration and types of consent (e.g.,specific, extended or unspecified), and any access restrictions applied. 15 years
RESEARCH INVOLVING GMOs
Records relating to managing Genetically Modified Organisms (GMO) or other material requiring biosafety provisions, while being used in specific research projects. Includes applications and assessments of Notifiable Low Risk Dealings (NLRDs), ongoing management of biosafety material. 8 years
RESEARCH INVOLVING ANIMALS
Records documenting the management and care of animals in the institution's custody, as required under the Australian Code for the Care and Use of Animals for Scientific Purposes, the Prevention of Cruelty to Animals Act and Regulations and associated codes of practice. Includes information about the acquisition of animals, scientific procedures or research projects using animals, number and species of animals held, number and species of animals removed from the premises or destroyed, and records of any breeding conducted. 7 years
RESEARCH INVOLVING OTHER SPECIMENS
Records relating to the management and administration of organic and inorganic specimens that are not derived from humans or animals, and which do not have any biosafety provisions and are held by the institution. Includes acquisition records, records relating to a specimen's condition and use in research projects, interventions undertaken on the specimen and destruction of the specimen or removal from the institution. 7 years
Top of PageSection 7 - Definitions
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- part of genetic research, including gene therapy;
HUMAN BIOSPECIMENS
*EXCEPTIONS TO DATA RETENTION TABLE: