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.

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.

2017-01-06