Harmonising the approach to VeDDRA coding workshop

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Kuupäev

Kolmapäev, 27 november 2013, All day

Asukoht

European Medicines Agency, Amsterdam, the Netherlands

The workshop will provide an opportunity for the regulators and industry to gain hands-on experience using VeDDRA to code adverse event reports and to strengthen the harmonised approach for use of VeDDRA coding terminology.

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