Mabel Adams Posted March 29 Share Posted March 29 I see TJC standard QSA.05.06.01 now says: Each day the procedure is performed, and when a new lot of reagents is first used, the laboratory tests at least one vial from each lot number of antisera, reactive cells, and reagents for reactivity. The reactivity results are documented. Note: This testing includes positive and negative reactivity when recommended by the manufacturer. We have always thought that JC requires QC on all open vials even if they are the same lot number. Does anyone know when this changed? Or is there a different standard that contradicts it? Link to comment Share on other sites More sharing options...
Solution Cliff Posted March 29 Solution Share Posted March 29 Yes, it did change. I cannot remember when. It made a huge difference for us. Mabel Adams 1 Link to comment Share on other sites More sharing options...
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