Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 January 2020

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

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Date

Pirmadienis, 13 Sausis 2020, 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.

Please note that this meeting will take place at EMA's temporary premises in the Spark building, not the EMA building in Amsterdam Zuidas.

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