Research Involving Washington Center for Bleeding Disorders (WACBD)

The ÌìÃÀÓ°ÔºIRB has agreed to provide IRB review and oversight of some research in which WACBD is engaged. This is because of the longstanding and intertwined relationship between WACBD (previously a part of Bloodworks Northwest) and ÌìÃÀÓ°Ôºhematology researchers, and because ÌìÃÀÓ°Ôºis often engaged in WACBD research.

WACBD may optionally obtain review from the ÌìÃÀÓ°ÔºIRB for all research in which it is engaged, except research that:

  • Is industry sponsored, or
  • Requires the use of the Exception to Informed Consent mechanism, or
  • Is cancer-related and involves more than minimal risk, or
  • Involves WACBD as the lead institution for multi-institutional research for which Single IRB review is required except when all institutions are other local institutions with which ÌìÃÀÓ°Ôºhas standing reliance agreements (e.g. Fred Hutch).

What to do if ÌìÃÀÓ°Ôºwill do the review

  1. Submit a ÌìÃÀÓ°ÔºIRB application in the Zipline system. Be sure to:
  2. The ÌìÃÀÓ°ÔºIRB will review and approve the overall protocol. This is not yet approval for the involvement of WACBD. After the ÌìÃÀÓ°ÔºIRB has approved the overall protocol, HSD’s Reliance Team will work with you to approve the addition of WACBD to the ÌìÃÀÓ°Ôºapplication.
  3. After ÌìÃÀÓ°ÔºIRB approval for WACBD has been obtained, you are responsible for:
    • Informing WACBD of UW’s approval for WACBD.
    • Informing WACBD investigators about any conditions of the IRB approval.
    • Informing WACBD investigators about their obligation to comply with ÌìÃÀÓ°ÔºIRB reporting requirements about noncompliance, complaints, problems, etc., although such reports must be submitted by you to the ÌìÃÀÓ°ÔºIRB.
  4. WACBD investigators remain responsible for obtaining any applicable ancillary reviews from WACBD. For example, Financial Conflict of Interest (FCOI) review.