European Medicines Agency publishes policy on communicating safety issues for human medicines
20/07/2010 - A new policy on communicating safety-related issues on medicines for human use has been published by the European Medicines Agency (EMA). The policy describes the various communication tools that are used. This includes the criteria for communicating on specific issues, the preparation and publication of communication material (including roles and responsibilities), the timing of the publication, how we work with the EU Regulatory Network and how we share communications material with other regulatory authorities both in Europe and beyond.
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