Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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The recovery of the standard has shifted. standardizaton of the immuno protein calibrator set has been re-established to ifcc reference preparation for plasma proteins bcd-470. this has caused a shift in quality control results and paitent results for igg iga trf and igm.