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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Allele information on the lot specific user document ssp-001l-010-ws-00 revision 0 (worksheet) is missing and may cause incorrect typing informaion for analysis completed manually. typing analysis using hla fusion software is not impacted by this issue.