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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Using f8 key in the erm session to add a combined test can result in the modification of the value of a result that has already been entered for a test of the request. this could only occur if the combined test added by f8 includes at least one test with the "duplicate result" property set to yes.