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.
데이터 추가 비고
원인
In the physician's intent workspace users manually enter the presribed dose/ fraction and the planned no. fractions (planned number of fractions) while aria calculates the planned total dose. this is done by storing the above values in a table in the database. it was identified that incorrect values were being stored for planned no. fractions leading to an unexpected calculation.