Updated guideline on data elements for electronic submission of AEs relating to VMPs

14 April, 2016

Following the implementation of VICH guidelines (GL30, GL35 and GL42), the “Guideline on data elements for the electronic submission of adverse reaction reports related to veterinary medicinal products authorised in the European economic area (EEA) including message and transmission specifications” has been updated slightly (Link). See details in the version history, page 52.

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