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Commission Implementing Regulation (EU) 2017/12 regarding the form and content of the applications and requests for the establishment of maximum residue limits in accordance with Regulation (EC) No. 470/2009 of the European Parliament and of the Council.

Country
Type of law
Regulation
Source

Abstract
This Regulation concerns the form and content of the applications and requests for the establishment of maximum residue limits in accordance with Regulation (EC) No. 470/2009 of the European Parliament and of the Council. An application or a request for the establishment of maximum residue limits (MRLs) shall be submitted to European Medicines Agency (EMA) electronically.
Date of text
Repealed
No
Serial Imprint
Official Journal of the European Union L 4, 7 January 2017, pp. 1-7.
Source language

English

Legislation Amendment
No