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Regulation No. 21 of 2005 of Minister of Agriculture of Estonia on Requirements and Procedure for the Use of Medicinal Products and Medicated Feed for the Prevention and Treatment of Animal Diseases

Country
Estonia
Type of law
Regulation
Date of original text
Source
FAO , FAOLEX
Abstract
This Regulation establishes requirements and procedure for the use of medicinal products and medicated feed for the prevention and treatment of animal diseases. The use of medicinal products and medicated feedingstuffs means their prescription, dispensing, storage and administration to animals and keeping records of these operations. The requirements laid down in this Regulation protect consumers of food of animal origin from health problems caused by the treatment of animals and prevent other disorders in humans or animals. More specifically, the Regulation provides for requirements for medicinal products and medicated feedingstuffs used; requirements for prescribing medicinal products and medicated feedingstuffs; requirements for dispensing medicinal products to keepers; requirements for storage of medicinal products and medicated feedingstuffs; requirements for administration of medicinal products and medicated feedingstuffs; procedure for prescribing medicinal products and medicated feedingstuffs; procedure for dispensing medicinal products; procedure for administration of the medicinal product; and keeping track of medicines.
Attached files
http://faolex.fao.org/docs/pdf/est196373.pdf
Web site
http://www.riigiteataja.ee
Date of consolidation/reprint
Repealed
No
Serial Imprint
RTL 2005, 27, 380
Source language

English

Legislation Amendment
No
Original title
Eesti p llumajandusministri 2005. aasta m rus nr 21 Ravimite ning ravims tade loomahaiguste ennetamiseks ja raviks kasutamise tingimused ja kord
Implements
Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products.
Directive 2003/74/EC of the European Parliament and of the Council amending Council Directive 96/22/EC concerning the prohibition on the use in stockfarming of certain substances having a hormonal or thyrostatic action and of beta-agonists.
Directive 2004/28/EC of the European Parliament and of the Council amending Directive 2001/82/EC on the Community code relating to veterinary medicinal products.
Regulation (EC) No. 470/2009 of the European Parliament and of the Council laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No. 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No. 726/2004 of the European Parliament and of the Council.
Commission Directive 2009/9/EC amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use.
Commission Regulation (EU) No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin.
Council Directive 90/167/EEC laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community.
Council Directive 96/22/EC concerning the prohibition on the use in stockfarming of certain substances having a hormonal or thyrostatic action and of -agonists.