Difference between revisions of "Research ethics"
m (→Ethical guidelines) (Tag: Visual edit) |
m (→Open access) (Tag: Visual edit) |
||
| Line 44: | Line 44: | ||
== Open access == | == Open access == | ||
| + | INformation about the UIO's open access policy in Norwegain: https://www.uio.no/for-ansatte/arbeidsstotte/forskningsstotte/kommunikasjon/kanaler-og-profilering/open-access/ | ||
Revision as of 13:44, 22 April 2022
Research ethics are good scientific practices and all employees at UIO and NCMM should have a high degree of awareness on the ethical aspects of their research. At NCMM the group leaders govern the responsibility for good scientific practices in line with the UIO policy.
UIO's10 commandments for ethical practices
Contents
Documentation of research
- Lab books- At NCMM we use numbered laboratory journals to document experiments. The books must be signed out and returned to Carlos: c.r.rodriguez@ncmm.uio.no
- Project tracking- It is important to store raw data, document procedures used and handling of data and material in agreement with the group leader
Data policy
- You can find Checklist for processing data here
- Key elements in an agreement for transfer of material by UiO here
- Form for subject identity list and list of trial subjects here
Forskpro
Is a registry UiO uses for overview of ongoing research projects. Here all medical and health research projects carried out at UiO should be registered. This also include other research projects if your unit at UiO is using Forskpro. Since NCMM is using Forskpro all projects must be registered.
How to register in Forskpro
For help with Forskpro contact Katrine Ore
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 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 some links to the most frequently used at NCMM.
Overview over approvals needed in medical research
- The regional ethics comity for medical research REK
- Norwegian Data Protection Authority
- Norwegian Food Safety Authority for approval for using research animals FOTS(Norwegian)
- Norwegian Directorate of Health GMO
Open access
INformation about the UIO's open access policy in Norwegain: https://www.uio.no/for-ansatte/arbeidsstotte/forskningsstotte/kommunikasjon/kanaler-og-profilering/open-access/
