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Guideline on good pharmacovigilance practices (GVP) - Module VI – Collection, management and submiss
Revision 2 of the guideline on good pharmacovigilance practices, Module VI, Collection, management and submission of reports of suspected...
Guideline on requirements for the production and control of immunological veterinary medicinal produ
This document provides information on items to be considered for the production and control of all immunological veterinary medicinal...
What’s new in Pharmacovigilance? QPPV update (Issue 2, July 2017)
The second issue provides you with information on recent developments in EU Pharmacovigilance, relating to medicines for human use, and...
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