Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 June 2017

EventHumanPharmacovigilance

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Date

Τρίτη, 6 Ιούνιος 2017, Ολοήμερο

Τόπος

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.

Documents

Agenda - PRAC draft agenda of meeting 6-9 June 2017

Draft Reference Number: EMA/PRAC/355498/2017

English (EN) (698.07 KB - PDF)

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Minutes of the PRAC meeting 6-9 June 2017

Adopted Reference Number: EMA/PRAC/478147/2017

English (EN) (891.13 KB - PDF)

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