Difference between revisions of "Research ethics"
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* Project tracking - It is important to store raw data, document procedures used and handling of data and material in agreement with your group leader. | * Project tracking - It is important to store raw data, document procedures used and handling of data and material in agreement with your group leader. | ||
==Data policy== | ==Data policy== | ||
− | * [https://www.uio.no/english/for-employees/support/research/research-data-management/index.html Storing and handling of research data] | + | * [https://www.uio.no/english/for-employees/support/research/research-data-management/index.html Storing and handling of research data]. |
− | * | + | * [https://www.uio.no/english/for-employees/support/research/quality-system-for-health-research/procedures/index.html#toc6 Checklist for processing data]. |
* Key elements in an agreement for transfer of material by UiO [https://www.uio.no/english/for-employees/support/research/quality-system-for-health-research/procedures/index.html#toc6 here] | * Key elements in an agreement for transfer of material by UiO [https://www.uio.no/english/for-employees/support/research/quality-system-for-health-research/procedures/index.html#toc6 here] | ||
* Form for subject identity list and list of trial subjects you find under appendices at this page [https://www.uio.no/english/for-employees/support/research/quality-system-for-health-research/procedures/procedure-6/ here] | * Form for subject identity list and list of trial subjects you find under appendices at this page [https://www.uio.no/english/for-employees/support/research/quality-system-for-health-research/procedures/procedure-6/ here] |
Revision as of 13:22, 7 July 2023
Research ethics is good scientific practice. All employees at NCMM shall have a high degree of awareness on the ethical aspects of their research. At NCMM the group leaders are responsible for ensuring good scientific practice in their group, in line with the UiO policy.
UiO's10 commandments for ethical practices
Contents
Open access
UiOs Open Access policy is in accordance with the Norwegian government's guidelines: NCMM staff "shall undertake to do their best to ensure that scientific articles deposited into the institutional repository can be made openly available as soon as possible".
Researchers at NCMM/UiO "shall ensure that a full text version of all scientific articles is submitted to the institutional repository."
All researchers submit their articles in Cristin, with transfer to DUO research archive. More on Open access from the University Library
Documentation of research
- Lab books - NCMM uses numbered laboratory journals to document experiments. The books must be signed out and returned to Carlos Rodríguez.
- Project tracking - It is important to store raw data, document procedures used and handling of data and material in agreement with your group leader.
Data policy
- Checklist for processing data.
- Key elements in an agreement for transfer of material by UiO here
- Form for subject identity list and list of trial subjects you find under appendices at this page here
Forskpro
Forskpro is a UiO registry used to obtain an dynamic overview of all ongoing research projects. All medical and health research projects carried out at UiO should be registered.
How to register in Forskpro
For help with Forskpro contact Medical faculty research administration
Authorship
As a general rule, NCMM aims to follow the Vancouver convention on authorship as closely as possible.
Ethical guidelines
We expect all members of NCMM to be honest in scientific research and communications and work within the scope of the UiO research ethics framework.
- Medical research
- Ethical guidelines
- Research data and data management
- Procedures for UiO’s quality system for medical and health Research (REK)
Approvals and authorizations
Certain types of research needs approvals and authorization from governmental entities and here are links to those most relevant at NCMM.
Overview of approvals needed in medical research
- The regional ethics comity for medical research REK
- Norwegian Data Protection Authority
- Routines for processing personal data in research projects
- Norwegian Food Safety Authority for approval for using research animals FOTS(Norwegian)
- Norwegian Directorate of Health GMO