Tri- Council Policy Statement on Research involving Human Subjects (TCPS2) Section A. Research Requiring REB Review

Good Clinical Practice: Consolidated Guideline; ICH Topic E6 Article 4.4 Communication with IRB/IEC/REB

CIHR Best Practices for Protecting Privacy in Health Research

Guidelines for conducting research in Indigenous Communities

Research Proposal/Protocol

Guidance-Document-HREB-General-Application

Guidance-Document-HREB-Secondary-Use-Application

Guidance Document HREB Clinical Trial Application Part A

Guidance Document HREB Clinical Trial Application Part B

Guidance Document Clinical Trials via the Researcher Portal

HREB Consent Guidelines

Glossary of Lay Terms for use in Informed Consent Forms

Participating in Research – Educational Documents

HREB Non-Clinical Trial Consent Form

HREB Genomics Consent Form

HREB Optional Study Consent Form

HREB Clinical Trials Consent Form

HREB Clinical Trials Consent Addendum Form

HREB Pregnancy Follow-Up Consent Form

HREB List of Variables

HREB Advertising Template

Oath of Confidentiality

Family physician form letter

Receipt for expenses form

HREB Annual Report 2024-2025

Metrics Q4 2025-2026

HREA Activity Plan 2023-2026

HREA Activity Report 2024-2025

Clinical Trials Ontario (CTO) report (2018)

• CTO Report
• CTO Summary
• HREA Action Plan