Status: draft (consultation open)
Consultation start date: 31/03/2015
Consultation end date: 30/06/2015
The aim of the current question-and-answer document is to provide clarification and to harmonise the use of the 'Guideline on the environmental risk assessment of medicinal products for human use' (EMEA/CHMP/SWP/4447/00).
Posted on the EMA website on 31 March 2015
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