Report EMA meeting


The European Medicines Agency has hosted a second workshop on the changes to the safety-monitoring of medicines in Europe, where it heard the expectations from patients, consumer groups, healthcare professionals and the pharmaceutical industry. ENFA representative was also present there.

The second stakeholder forum on the implementation of the new pharmacovigilance legislation, which took place on Friday 17 June 2011, involved discussions between the Agency, key stakeholder groups and medicines regulatory authorities from the European Union (EU) Member States.

The full report can be read here


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