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

• Date:
  Wednesday, 16 June 2010
• 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

Minutes of the tenth EMA human scientific committees' working party with patients' and consumers' organisations (PCWP) meeting of 16 June 2010

Reference Number: EMA/405307/2010

Presentation: Applied ethics & societal aspects in applied human pharmacology

Presentation: Direct patient reporting of adverse drug reactions: a 15-country survey

Presentation: 2009 report on the interaction with Patients’ and Consumers’ Organisations