New EMA Draft Guideline for Environmental Risk Assessment of Medicinal Products – PRECLINICAL SCIENCE

New EMA Draft Guideline for Environmental Risk Assessment of Medicinal Products

By Geertje Lewin

Posted January 15, 2019

In Legislative change

At the end of 2018, the European Medicines Agency published the new draft Guideline on the environmental risk assessment of medicinal products for human use for public consultation. Deadline for comments will be 30 June 2019.

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