Résumé
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.
Informations générales
-
État actuel: AnnuléeDate de publication: 2009-10Stade: Annulation de la Norme internationale [95.99]
-
Edition: 1
-
Comité technique :ISO/TC 215ICS :35.240.80
- RSS mises à jour
Cycle de vie
Vous avez une question?
Consulter notre Aide et assistance
Service à la clientèle
+41 22 749 08 88
Horaires d’ouverture:
De lundi à vendredi - 09:00-12:00, 14:00-17:00 (UTC+1)