Resources
Study Feasibility Assessment
Templates
- Abbreviated CV for Research - Sample Template 2015-04-01
- Addendum Informed Consent 2016-01-08
- Advertisement Template 2019-01-09
- Access Personal Health Information Consent Form *Please remember to include Encounter # and MRN # before sending to health records*
- Consent Case Reports 2021-06-21
- Consent Database Registry Studies 2020-11-19
- Consent Genetic Template 2021-05-13
- Consent Interventional Trials Template 2021-07-14
- Consent Non-Interventional Studies Template 2021-03-01
- Consent Pregnant Partner Template 2021-06-21
- Researchers Commitments: Site Investigator
Guidance Documents
- Consent Preparation and Use 2015-04-01
- EAS form F2 section RMU wording 2015-04-01
- Radiological Review Information
- Research Protocol Guidelines 2015
Reviewer's Assessment Forms
- Reviewer's Assessment Clinical Trials Protocol 2015-04-01
- Reviewer's Assessment Non-Interventional Trials Protocol 2015-04-01
- Reviewer's Assessment Risk 2015-04-01
- Reviewer's Assessment Form Consent 2015-04-01
- Risk Assessment Guide 2015-04-01
- Reviewer Assessments - Checklist for Methodology Review 2021-10-12
Resources
- Interagency Advisory Panel on Research Ethics (PRE)
- The Governance of Health Research Involving Human Subjects (HRIHS)
- Tri-council Policy Statement: Ethical Conduct for Research Involving Humans
- Good Clinical Practice: Consolidated Guideline
- Health Canada: Food and Drugs Act, Division 5
- World Medical Association Declaration of Helsinki
- The Belmont Report (USA)
- Nuremberg Code (USA)
- Code of Federal Regulations (USA)
- International Ethical Guidelines for Biomedical Research Involving Human Subjects
- Canadian Bioethics Society
- Office for Human Research Protections (USA)
Videos
- Informed Consent of Research Participants through REDCap (Access Passcode: 7CRh#!Uq)
- Indigenous Research Webinar