European Medicines Agency Human Scientific Committees' Working Party with Patients' and Consumers' Organisations (PCWP) plenary meeting with all eligible organisations

Date

Wednesday, 30 November 2011, All day

Location

European Medicines Agency, Amsterdam, the Netherlands

Day 2: This meeting includes an introduction from the new Executive Director. Some of the general issues for discsussion at the meeting are the implementation of the anti-falsification legislation; additional monitoring of medicines and direct patient reporting; legislation on information to patients; results of survey project on representativeness in Agency stakeholder groups; outcome of the scientific advisory group pilot phase; and process for re-evaluation of eligibility.Registration by invitation only.

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