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FAQ

c-IRB

  • Q1

    What is c-IRB?

    c-IRB has been implemented since 2013. When a multicenter trial is registered to c-IRB System, one of the 7 main IRBs is assigned to conduct a full-board review which will be completed in 20 days (sponsor time is excluded). After that, the review records and results are forwarded to sub-IRBs in all participating sites by the sponsor. Sub-IRBs conduct expedited review which will be completed within 10 days.

  • Q2

    What are the requirements for c-IRB review?

    It is applicable for multicenter trial that includes at least one site to be one of the main c-IRB review members.

  • Q3