ISO/TS 22224:2009 encompasses the electronic reporting of adverse reactions caused by drugs for human uses. Thus, other businesses relating to adverse events caused by blood transfusion, medical devices and veterinary drugs are excluded from the scope of ISO/TS 22224:2009.
Status : WithdrawnPublication date : 2009-10
Edition : 1
Technical Committee:Health informatics
A standard is reviewed every 5 years
Revisions / Corrigenda