Regulation on maximum allowed quantities of residues of pharmacologically active substances in veterinary medicinal products in products of animal origin.
Country
Type of law
Regulation
Abstract
This Regulation prescribes the detailed conditions (in terms of animal welfare issues, animal health and animal sanitary-veterinary requirements) to be met by facilities and equipment for holding and production of animals for the direct purpose of animal production.
This Regulation transposes the rules contained in the Table 1 of the Annex part of the Commission Regulation No. 37/2010 on pharmacological active substances and their classification in relation to the maximum permitted quantities of residues in food of animal origin.
The Annex is an integral part of this Regulation.
This Regulation transposes the rules contained in the Table 1 of the Annex part of the Commission Regulation No. 37/2010 on pharmacological active substances and their classification in relation to the maximum permitted quantities of residues in food of animal origin.
The Annex is an integral part of this Regulation.
Attached files
Web site
Date of text
Entry into force notes
This Regulation enters into force eight days after its publication in the Official Gazette.
Repealed
Yes
Publication reference
(Official Gazette 41/2014)
Source language
English
Legislation Amendment
No
Original title
Pravilnik o maksimalno dozvoljenim količinama rezidua farmakološki aktivnih supstanci veterinarskih ljekova u proizvodima životinjskog porijekla.
Implements