The Tri-Hospital Research Ethics Board (THREB) is a shared research ethics board serving Cambridge Memorial Hospital, Grand River Hospital and St. Mary's General Hospital. THREB reviews all research involving human subjects at these hospitals, except for research reviewed by an alternate Board of Record for one of the hospitals (e.g. the Ontario Cancer Research Ethics Board).
In order to facilitate this review, all the necessary documentation must be included in the application (see forms below).
THREB meets the first Wednesday of the month except during July and August. A completed application package including the signed original and five copies (six copies in total) must be received by the second Wednesday of the month prior to the meeting date. A checklist outlining the required steps is included as the first part of the application form.
Minimal risk studies that may receive delegated (expedited) review instead of full board review have no deadline for receipt.
The primary responsibility of the THREB is to make decisions concerning the ethical acceptability of research proposed by the hospital(s), by researchers having an association with the hospital(s), or any research involving patients or staff at the hospital(s). For purposes of review by THREB, research is defined as "an undertaking intended to extend knowledge through a disciplined or systematic investigation" (Tri-Council Policy Statement 2).
THREB is mandated to approve, reject, propose modifications to, or terminate any proposed or ongoing research involving human subjects that is conducted within the hospitals, again with the exception of research reviewed by an alternate Board of Record for the hospital(s). THREB complies with guidelines from
- The Tri-Council Policy Statement Ethical Conduct for Research Involving Humans 2 (2010)
- The Good Clinical Practice: Consolidated Guideline of the International Conference on Harmonization
- Division 5 Health Canada Food and Drug Regulations
- Relevant Canadian health and privacy legislation
THREB also endeavours to facilitate compliance with the human subject requirements of two US federal agencies: The Food and Drug Administration and the Office for Human Research Protections, US Dept of Health and Human Services.
Additional administrative review
While THREB reviews all research, administration departments at each hospital also review research for financial, resource, and contractual implications (see administrative approval form application part 3).
Please note: Each hospital has a unique process for administrative review and approval. This process must be completed before THREB review can be initiated. It is up to the Investigator to make contact with the relevant institutions to determine their requirements. Contact information for administrative review at the three hospitals can be found below and in the administrative approval form (application part 3).
Cambridge Memorial Hospital
Sandra Hett, Vice President, Clinical Programs and Chief Nursing Executive
700 Coronation Boulevard, Cambridge, Ontario N1R 3G2
Telephone: 519-621-2333 extension 2416
Grand River Hospital
Sarah Laferriere, Research Office Administrator
Grand River Hospital
835 King Street West, Kitchener, Ontario, N2G 1G3
Telephone: 519-749-4300 extension 2876
St. Mary's General Hospital
Melody Vallerand, Administrative Assistant to VPs and CFO,
911 Queen’s Boulevard, Kitchener, Ontario N2M 1B2
Both the administrative review and the research ethics board review must be completed and any outstanding issue resolved prior to the research being initiated.
For more information, or to send an application and other forms, contact:
Shelley Croth, THREB Administrative Coordinator, Tri-Hospital Research Ethics Board
Grand River Hospital, Kaufman Building room K415,
835 King Street West, Kitchener, ON N2G 1G3
Phone: 519-749-4300, extension 5367
You can reach the THREB Chairperson, Dr. Michael D. Coughlin at: email@example.com
More information is available under the following links:
- General information and guidelines for investigators
- Meeting dates for 2016
- Terms of reference
- Procedures for renewal and continuing review (SOP#4.4)
- Procedures for reporting SAEs and unanticipated problems (SOP#4.5)
- Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS2) (opens in new window)
- Good Clinical Practice Guidelines (GCP) (opens in new window)
- Website to access TCPS2 Tutorial (opens in new window)
In general, the THREB requires the original and five copies (six packages in total) of all documents that must be reviewed. To provide sufficient time for review, completed application packages and other items for review must be received by the second Wednesday of the month prior to the THREB meeting date. Please email an electronic copy of the submission to firstname.lastname@example.org.
- Application form for project review (revised October 2016)
- Application for retrospective review of health records (revised October 2016)
- Administrative approval form (application - part 3) (revised October 2016)
Forms for continuing review