(a) Blood collection facilities licensed pursuant to section 19a-36-F2 shall conduct all donor testing at a duly licensed clinical laboratory.
(b) Blood and blood components collected shall be tested according to the requirements of 21 CFR 610.40 and 21 CFR 640.5, as amended from time to time.
(c) All donor eligibility testing conducted at a reference laboratory shall be conducted by personnel licensed as required in the state where testing occurs.