Has anyone come up with a way to comply with the "peer review" in AABB Standard 8.2 (Transfusing facilities shall have a peer-review program that monitors and addresses transfusion practices for all categories of blood and blood components.) other than presenting data at Transfusion Committee Meetings?
Carrie - would you consider sharing your plan - or at least a high level summary of your rationale for the number and distribution of samples / cells tested?
Thanks!
Use of either pHix or Buffering solution as described is outside of IFU and would require extensive in-house validation to support their use. Not only would you have to provide "in-use" testing, you would also have to determine stability data.
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