Research forms, guidance notes and templates

Information to guide you in the process of completing the Amendment request section of the Post-Approval Research Ethics Application form correctly.

Information to guide you in completing the Renewal request section of the Post-Approval Research Ethics Application form correctly.

Information to guide you in completing the Close-out request section of the Post-Approval Research Ethics Application form correctly.

Information to report unanticipated problems including local and non-local serious adverse events.

Information for investigators on requirements for submissions concerning a protocol deviation that had not received prior approval by the Fraser Health Research Ethics Board.

This template is intended to assist investigators in producing tissue consent forms which meet the FHREB’s requirements regarding studies involving the optional acquisition and possible banking of tissue.

Template is intended to assist investigators in producing assent forms which meet the Fraser Health Research Ethics Board requirements. This form is for children aged 7-13 years.

Template for consent to collect medical information regarding pregnancy, birth, and infant health from a female partner impregnated by a male participant in an experimental clinical trial.

Template for writing a research protocol for research involving human participants.

Research participants may use this form to submit complaints from their participation in research studies conducted at our sites.

Principal investigators planning to conduct research that requires the provision of services, access to personal information or site resources must use this form to obtain the applicable department/area’s permission, regardless of funding.

Researchers may contact our Information Management Department for services required for the conduct of their research study.

Overview of the health records approval process.