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European Union Medicines Agency

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Preview of List item EU VICH adverse event report implementation guide (PDF/1.2 MB) AdoptedFirst published: 23/11/2021 Legal effective date
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List item EU VICH adverse event report implementation guide (PDF/1.2 MB) AdoptedFirst published: 23/11/2021 Legal effective date (eu-vich-adverse-event-report-implementation-guide_en.pdf)

1.2 MBEuropean Medicines AgencyEN 44 pages
The European Medicines Agency (EMA) has published the EU VICH adverse event report implementation guide, which provides guidance on reporting adverse events
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