Pharmacovigilance Risk Assessment Committee (PRAC): 2-5 May 2017

Dutch is available via eTranslation, the European Commission's machine translation service.

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Date

dinsdag, 2 mei 2017, Hele dag

Locatie

European Medicines Agency, Amsterdam, the Netherlands

The Pharmacovigilance Risk Assessment Committee (PRAC) is the committee that is responsible for assessing all aspects of the risk management of medicines for human use.

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