Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 February 2016

EventHumanPharmacovigilance

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Date

måndag, 8 februari 2016, Hela dagen

Plats

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 8-11 February 2016

Draft Reference Number: EMA/PRAC/94187/2016

English (EN) (481.74 KB - PDF)

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Minutes of the PRAC meeting 08-11 February 2016

Adopted Reference Number: EMA/PRAC/251925/2016

English (EN) (960.64 KB - PDF)

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