Draft Regulation – Methodological Principles for the Risk Assessment and Risk Management Recommendations for the Maximum Residue Limits

This Regulation sets out the methodological principles for the scientific risk assessment and risk management recommendations referred to in Articles 6 and 7 of Regulation (EC) No 470/2009 that shall be applied by the European Medicines Agency when preparing opinions on the maximum residue limits of pharmacologically active substances which may be permitted in food of animal origin.
Deadline: 13 December 2017
Website: https://ec.europa.eu/

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