Research at Northern Health requires two approvals to proceed:
- Research Ethics Approval
- Northern Health Operational Approval
Research ethics and operational approvals can be pursued simultaneously. Once the conditions for research ethics and operational approval are met, a letter of approval from the Research Review Committee will be emailed to the Principal Investigator and the Northern Health managers who provided operational approval for the research.
All research conducted within or for Northern Health (NH) must be reviewed and approved by the Northern Health Research Review Committee (RRC). The RRC is mandated by NH policy to approve, reject, propose modifications to or terminate any proposed or ongoing research involving humans that is conducted: in NH facilities/programs; by NH staff or physicians; or with NH staff, physicians and/or patients.
The RRC’s function is to ensure that ethical principles and standards respecting the personal welfare and rights of research participants have been recognized and accommodated. The RRC is also directed to consider the impact of the research on the NH organization.
The Committee follows NH Research Policy and Principles, the Freedom of Information and Protection of Privacy Act (FIPPA) and the (TCPS-2)Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans.
Please refer to the Application Guidelines for important information regarding the completion of your application. The guidelines contain instructions for submitting your application. This application covers both research ethics and operational approval requirements.
Refer to the Research Risk Assessment Guidelines to complete Section A of your application and find information to help you obtain operational approval.
If your research is affiliated with the University of Northern British Columbia, you can submit your completed UNBC Research Ethics Board New Application Form together with the Northern Health Operational Approval form. You are required to submit your application to both UNBC and Northern Health).
Visit the UNBC Office of Research at www.unbc.ca/research for information about their research services and Research Ethics Board.
- If the project requires secondary data from Health Information Management Services (HIMS - Health Records) a Data/Chart Request form, signed by the HIMS Department, must be submitted with your application.
- For regional/multi-site studies in Northern Health contact Dee-Ann.Stickel@northernhealth.ca
- For studies involving the University Hospital of Northern BC, Prince George site only contact firstname.lastname@example.org
UBC and the Health Authorities have developed a process for ethical review of these resident, intern and summer medical student research projects.
Refer to the UBC Guidance Note (posted under both the UBC BREB and CREB) for the initial application review process involving studies in Northern Health. The process involves an initial application to the UBC RISe system that will be reviewed by both UBC and Northern Health, and the completion of the Northern Health Application for Operational Approval form to be submitted to email@example.com.
You can pursue research ethics approval and operational approval simultaneously.
If your research requires ethics approval from multiple organizations (Universities and Health Authorities) in BC, you may be able to proceed with a Harmonized ethics review process.
The process begins with a conversation with your home Institution’s Research Ethics Office and the completion of the Cover Sheet for Harmonized Ethics Review. A flowchart of the process for review of minimal risk and above minimal risk studies can be found on the BC Ethics Harmonization Initiative Resources Page.
If you obtain research ethics approval through a Harmonized Ethics Review, your study will still require operational approval before it can proceed in Northern Health.
For operational approval, complete the Application for Operational Approval form and submit it to firstname.lastname@example.org. You can pursue research ethics approval and operational approval simultaneously.
Learn more about the BC Ethics Harmonization Initiative.
- Canadian Institutes of Health Research (CIHR)
- Natural Sciences and Engineering Research Council of Canada (NSERC)
- Social Sciences and Humanities Research Council (SSHRC)
- Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS2)
- National Council on Ethics in Human Research (NCEHR)
- Canadian Association of Research Ethics Boards (CAREB)
- Alberta Research Ethics Community Consensus Initiative (ARECCI)
- Ethics at the Canadian Institutes of Health Research (CIHR)
- CIHR Ethics
- National Aboriginal Health Organization (NAHO)
- Canadian Institutes of Health Research (CIHR)
- Institute of Aboriginal People's Health (IAPH)
- CIHR Guidelines for Health Research Involving Aboriginal People (2007-2010)
- Freedom of Information and Protection of Privacy Act Province of British Columbia (FOIPPA)
- The entire FOIPP Act
All studies must have approval to conduct research at Northern Health from the Manager/Director of each department who has appropriate authority to assess the impact and to support the dedication of resources (e.g., human or financial resources, space in the facility) to the research (if applicable).
In addition to assessing the impact and dedication of resources, the Manager/Director will consider the benefits of the research and how the results can be used in Northern Health. Projects may require approval from more than one Manager or Director.
To obtain operational approval, complete the Application for Operational Approval for Research form and submit it to email@example.com
Refer to the Northern Health Operational Approval for Research Projects for information on the process for obtaining operational approval, who can grant operational approval, and the roles and responsibilities of the Researcher and the Northern Health Approval Manager.
- Kirsten Thomson, Regional Director, Risk and Compliance, NH
- Linda Axen, Regional Manager, Policies and Clinical Practice Standards, NH
- Sam Milligan, Carrier Sekani Family Services
- Damen DeLeenheer, Clinical Educator, NH
- Robert Pammett, Research and Development Pharmacist – Primary Care, NH
- Kerensa Medhurst, BC Cancer Agency
- Tanis Hampe, Regional Director, Quality & Innovation, NH
- Dr. Andrew Gray, Medical Health Officer, NH
Tammy Hoefer, Regional Manager Innovation & Development Commons, NH
|Applications Deadline||Meeting Date|
|Jan 12, 2018||Jan 25, 2018|
|Feb 9, 2018||Feb 22, 2018|
|Mar 9, 2018||Mar 22, 2018|
|Apr 13, 2018||Apr 26, 2018|
|May 11, 2018||May 24, 2018|
|June 15, 2018||June 28, 2018|
|Sept 14, 2018||Sept 27, 2018|
|Oct 12, 2018||Oct 25, 2018|
|Nov 9, 2018||Nov 22, 2018|
*Applications submitted by the deadline will be reviewed within 2 weeks.