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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This issue concerns an issue with the evaluation of biological clinical goals in raystation 3.0. raystation 3.5 raystation 4.0 raystation 4.5 raystation 4.7 and raystation 5. biological clinical goals for an adapted plan based on another planning ct than the original planning ct will show incorrect values.