We are also on HCLL and Multi-facility...our process is to have each facility create a HCLL only registration with a unique name that has no information indicating it is a CAP specimen. The donor numbers are unique for each site too.
We did get a CAP deficiency for this. We test the controls from the old lot with the anti-D and Indicator cells from the new lot prior to the new lot being put into use.
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