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Q&As Article 57(2): Electronic submission of information on medicinal products for human use by

Electronic submission of Article 57(2) data Questions & Answers (Q&As).

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Guideline on good pharmacovigilance practices (GVP) - Module VI – Collection, management and submiss

Guideline on requirements for the production and control of immunological veterinary medicinal produ

What’s new in Pharmacovigilance? QPPV update (Issue 2, July 2017)

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