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ISO/TS 22224:2009

Health informatics -- Electronic reporting of adverse drug reactions

General information
Withdrawn from 14.12.2015
Directives or regulations
None
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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.
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