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Home...Osler Research Institute for Health InnovationResearch Ethics BoardStandard Operating Procedures

Standard Operating Procedures

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Osler's REB follows a set of Canadian Standard Operating Procedures (SOPs). In doing so, we are helping facilitate a single standard for REBs in Canada.

Our SOPs are available via open access and compliant with applicable Canadian and US regulatory and ethics guidance criteria.

For institution-specific requirements, please contact us.

100 General Administration (101-108)

SOP #VersionTitle

101.002

Authority and purpose

102.002

Research requiring REB review

103.002

Training and education

104.002

Management of REB office personnel

105A.002

Conflicts of interest - REB members and REB office personnel

105B.002

Conflicts of interest – researcher

105C.002

Conflicts of interest – organization

106.002

Signatory authority

107.002

Use and disclosure of personal information

108.002

Standard operating procedures maintenance

200 REB Organization (201-204)

SOP #VersionTitle

201.002

Composition of the REB

202.002

Management of REB membership

203.002

Duties of REB members

204.002

REB office personnel serving as REB members

300 Functions and Operations (301-303)

SOP #VersionTitle

301.002

REB submission requirements and administrative review

302.002

REB meeting administration

303.002

  • Document management
  • Addendum - document management

400 Reviews of Research (401-407)

SOP #VersionTitle

401.002

Delegated review

402.002

REB review decisions

403.002

Initial review - criteria for REB approval

404.002

Ongoing REB review activities

405.002

Continuing review

406.002

Research completion

407.002

Suspension or termination of REB approval

500 Reviews Requiring Special Consideration (501)

SOP #VersionTitle

501.002

REB review during publicly declared emergencies

600 REB Communication and Notification (601-602)

SOP #VersionTitle

601.002

Communication – researcher

602.002

Communication - research participants

700 Informed Consent (701)

SOP #VersionTitle

701.002

Informed consent form requirements and documentation

800 Responsibilities of Investigators (801)

SOP #VersionTitle

801.002

Research qualifications and responsibilities

900 Quality Management (901-902)

SOP #VersionTitle

901.002

Quality assurance inspections

902.002

External inspections or audits

903.002

Non-compliance

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