Workshop: User testing and how to review the data
Event
Date
- Friday, 23 November 2007, All day
Location
- European Medicines Agency, Amsterdam, the Netherlands
The EMEA and the Coordination Group for mutual recognition and decentralised procedures (human) (CMD(h)) held the second workshop on user consultation in the context of assessment of readability testing of package leaflets for medicines on 22 November 2007. The workshop, titled "User testing and how to review the data", was a follow-up from the first one held on 23 October 2006. Its aim was to review and bring together experience and expertise of European regulators with readability testing of the package leaflets by target patient groups.