These procedures are guidelines for medicinal and health research carried out at UiO. You will also find templates (forms and checklists) ready for use in the documentation of your project.
Procedure 1: Responsibility and delegation of tasks at UiO pursuant to the Health Research Act
The procedure describes the responsibilities of the University Director, the delegation of tasks to faculties and other levels in the organization that carry out medicinal and health research
Procedure 2: Responsibilities and tasks of the Principal Investigator (Project Manager), pursuant to the Health Research Act
The procedure describes the responsibilities and tasks of the Principal Investigator when managing medicinal and health research which does not involve any use of medicines or medical equipment on research subjects
Procedure 3: Responsibilities and tasks in connection with clinical trials of medicinal products
The procedure describes the responsibilities of the University Director (sponsor) and principal investigator in connection with clinical trials of medicinal products under the auspices of UiO.
Procedure 4: Responsibilities and tasks in connection with clinical trials of medical devices
The procedure describes the responsibilities of the University Director (sponsor) and principal investigator in connection with clinical trials of medical devices under the auspices of UiO.
Procedure 5: Use of human biological material for research purposes
The procedure describes responsibilities and tasks associated with research on human biological material.
Procedure 6: Storage and handling of research data
The procedure describes how research data should be stored and handled in ways that respect the privacy protection rights of the research subject.
Procedure 8: Reporting and handling deviations under the Health Research Act
The procedure describes how to report, handle and follow up on deviations in accordance with the Health Research Act