Pharmacovigilance Risk Assessment Committee (PRAC): 9-12 January 2017

EventHumanPharmacovigilance

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Date

Pirmadienis, 9 Sausis 2017, All day

Vieta

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 9-12 January 2017

Draft Reference Number: EMA/PRAC/816784/2016

English (EN) (579.25 KB - PDF)

Pirmą kartą paskelbta: Paskutinį kartą atnaujinta:
Rodyti

Minutes of the PRAC meeting 9-12 January 2017

Adopted Reference Number: EMA/PRAC/243286/2017

English (EN) (878.59 KB - PDF)

Pirmą kartą paskelbta: Paskutinį kartą atnaujinta:
Rodyti

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