Tenth EMA Human Scientific Committees' Working Party with Patients' and Consumers' Organisations (PCWP) meeting

Date

Wednesday, 16 June 2010, All day

Location

European Medicines Agency, Amsterdam, the Netherlands

The meeting covered the following topics: revision of the mandate and rules of procedure of the PCWP; the interaction between the Agency and health technology assessment bodies; the interaction between the Agency and patient & consumer organisations; direct reporting of adverse events by patients.

Documents

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