Guidelines & Templates
New Templates Available!
A single standardized consent template is used for both pediatric and adult studies.
OCREB requirements outlined in our Guidelines, Memos, and consent form templates remain in effect. This includes the pre-approval of all centre-specific consent forms without the requirement for OCREB review. For pre-approval memos specific to your centre or for any questions related to OCREB’s Guidelines, Memos, or templates, please contact the OCREB Research Ethics Officer.
Guidelines and Memos
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- OCREB Participant Reimbursement Guidelines
- Genetic Non-Discrimination Act (GNDA) Guidance for OCREB Reviewers
- Memo: Implementation of Team-based Consenting for Paediatric Studies Approved by OCREB
- Memo: Change in Consenting Practices for Paediatric Clinical Trials
- Memo: Wallet Card Template
- Memo: Pre-Screening Consents
- Memo: Consent Section on Participant Assistance (Use of Interpreters)
- Memo: DIL and Protocol Clarification Letters
- Guidance for Pre-Approved Administrative Changes
- Guidelines for Protocol Deviation Reporting
- Guidelines for Managing Conflict of Interest
- Guidelines for Providing New Information
Templates
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The OCREB consent template is a single standardized template for both paediatric and adult studies