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

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

Translate to Latvian | Important information about machine translation

Date

Pirmdiena, 9 Janvāris 2017, Visu dienu

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

Share this page