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Review Services

Canadian Review Services

Key Benefits

  • Three Canadian meetings a week
  • Largest AAHRPP-accredited Canadian REB
  • Official provincial recognition
  • Single submission process for Canada and U.S.

Overview of Canadian IRB/REB Services

Local Expertise

Membership includes Canadian citizens and residents, offering localized insight while ensuring compliance with Health Canada and privacy regulations.

Meeting Frequency

Advarra provides frequent review opportunities, with meetings every Tuesday, Wednesday, and Friday.

Extensive Reach

Advarra supports more Canadian sites than any other partner, offering the broadest provincial coverage and experience in the industry.

Accreditation and Recognition

As the largest central IRB/REB in Canada, Advarra holds AAHRPP full accreditation and official provincial recognition, offering trusted compliance with local requirements.

Cross-border Studies

Simplify reviews and save time with a single submission process for trials conducted in both the U.S. and Canada.

Turnaround Times
4–
business
days

New protocol and initial informed consent for multisite studies
(full board review)

1–
business
days

New protocols and initial informed consent for minimal risk review

1–
business
days

New site for a multisite study

Turnaround time is dependent upon complete and accurate submission of study documents. Any follow-up requiring a response may extend this turnaround time.

Interested in learning more about Advarra’s Canadian IRB/REB services for your clinical trials?

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