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
Agfa has determined that the current process allowing changes to be made to the impax cv reporting application content via rmat has the potential for misuse. errors may result from uncontrolled changes and these errors could lead to incorrect and clinically significant inaccuracies in the report.