EMA Focuses on New Legislation in 2012 Work Programme
The Agency's activities this year will concentrate on the implementation of the pharmacovigilance legislation and preparations for the new legislation on falsified medicines.
The European Medicines Agency's activities this year will concentrate on the implementation of the pharmacovigilance legislation and preparations for the new legislation on falsified medicines, according to the work programme 2012, published last week.
The document forecasts a stable number of applications for marketing authorisation for human and veterinary medicines in 2012. It states that the Agency will continue to review its activities and processes so that it can identify areas where efficiency gains, re-allocation of resources and reprioritisation of activities may be possible. This should put the Agency in a position to manage its increased responsibilities with existing resources.
In line with the road map implementation plan, the
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