At our laboratory, we have a policy to run 2 levels of QC after each reagent change, even if it’s same lot number. I can see if it’s a new lot and Sysmex has provided documentation on that, but with every, same lot # change seems excessive to me. Does anyone else do this? Is this required by any accrediting agency?
I’m a newbie Hematology supervisor so I’m looking at things with a fresh set of eyes, albeit a little rusty in Hem so I need the community help. Thanks for your response.