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.
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.
Title:
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:
European Union
Type of document:
Regulation
Date of text:
2017
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