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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For clients using a customized lab results ap macro or a micro results results ap macro in the patient report template there is a possibilility that the lab tests displayed may be only for the first order from the date range for the patient.