Policies
25.3 Research Integrity Policy
SOPs
SOP 502 Activities Requiring Research Ethics Board Review
SOP 505 Research Ethics Application Review Process
SOP 506 Research Ethics Boards Meeting
SOP 507 Documentation and Document Management
SOP 508 Ongoing Research Ethics Board Review Activities
SOP 512 Training and Education of Research Ethics Board Members and Office Personnel
SOP 513.1 Research Ethics Board - Delegated Review
SOP 513.2 Delegated Review - Delegated Responsibility to Research Ethics Board Office Personnel
SOP 515 Management of Research Ethics Board Office Personnel
SOP 516 Research Ethics Boards - Administrative Holds, Terminations and Suspensions of Approval
SOP 520 Research Ethics Boards – Signatory Authorities
SOP 523 Research Ethics Review Fees
SOP 524 Harmonized Research Ethics Review
SOP 525 Research Ethics Board Review During Publicly Declared Emergencies
SOP 527 Research Ethics Board - Uses and Disclosures of Personal Information
SOP 529 Conflicts of Interest (Research) – Researchers
SOP 530 Conflicts of Interest (Research) – Organization
SOP 531 Research Ethics Boards – Authority and Purpose
SOP 532 Research Ethics Boards - Policies and Procedures Maintenance
SOP 533 Composition of the Research Ethics Boards
SOP 534 Duties of Research Ethics Board Members
SOP 535 Management of the Research Ethics Boards
SOP 536 Research Ethics Board Office Personnel Serving as Research Ethics Board Members
SOP 537 Research Submission Requirements
SOP 538 Administrative Review and Distribution of Materials
SOP 544 Research Ethics Board Review Decisions
SOP 545 Initial Research Ethics Board Review - Criteria for Approval
SOP 546 Reconsiderations of Research Ethics Board Decisions and Appeal Process
Provincial Guidance
Research Ethics & Compliance including REBs support these statements and guidelines regarding the activities pertaining to public health surveillance.
Island Health REB Guidance
- Use of Form FDA 1572 - September 2022
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Island Health REBs Policy Statement for the use of Form FDA 1572
- Electronic Consent Guidance – September 2021
- Research Ethics Guidance – July 2021
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Research Ethics Guidance – Participant ID on Study Documents 20 July 2021
- Research Ethics Guidance – March 2020
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Remote Monitoring Guidance