Anvisningens framsida

Syfte

I det här dokumentet beskrivs processer och åtgärder ur olika användargruppers perspektiv relaterade till hantering av larm. Med hjälp av dokumentet kan kundernas IT-system vidareutvecklas så att användaren snabbt och lätt kan se läkemedelsverifieringsförfrågans informationsinnehåll och svaret i FiMVS-systemet samt om det är fråga om ett felmeddelande eller larm.

Revision history

  • Version 1.0 updated on 4th December 2020, initial document created, SOP included in the Quality Management System and the structure has been aligned with the SOP template. Changes introduced by EU Hub R1.8 have been addressed. The most significant change is that all alerts are now propagated to the OBP.
  • Version 2.0 updated on 3rd of May 2021, alert messages updated, The Swedish alert and exception messages by FiMVS have been adapted to be more understandable.
  • Version 3.0 updated on 8th of November 2021, changes made in two alert functionalities, Document type has been changed to work instruction. Changes introduced by FiMVS Core release 1.09 have been addressed. The functionalities regarding alerts NMVS_NC_PCK_19 and NMVS_NC_PCK_22 have been modified.