Pharmacovigilance Risk Assessment Committee (PRAC): 6-9 June 2016

EventHumanPharmacovigilance

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Date

Montag, 6 Juni 2016, Ganztägig

Ort

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 2016

Draft Reference Number: EMA/PRAC/231459/2016

English (EN) (501.72 KB - PDF)

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Minutes of the PRAC meeting 06-09 June 2016

Adopted Reference Number: EMA/PRAC/460046/2016

English (EN) (848.67 KB - PDF)

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