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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After exporting a plan created with the radiotherapy treatment planning software iplan rt dose to the record & verify system a user noticed that iplan rt dose exported a higher number of monitor units for patient irradiation than intended by the treatment plan.