National Office of Animal Health
...for the welfare of all animals

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Annual Report 2009/2010
Annual Report 2008/2009
Annual Report 2007/2008
Annual Report 2006/2007
Annual Report 2005/2006
Annual Report 2004/2005
Annual Report 2003/2004
Annual Report 2002/2003
Annual Report 2001/2002
Annual Report 2000/2001

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NOAH

the regulator

Animal medicines go through an extremely strict scientific assessment before they are allowed to be sold. The Veterinary Medicines Directorate (VMD) is the Department for Food, the Environment and Rural Affairs’s Executive Agency which is responsible for the evaluation and regulation of UK animal medicines and also grants the marketing authorisations for these products. Similar controls apply to medicines authorised across the EU through the European Medicines Agency (EMEA).

The VMD is advised by independent advisory committees including the Veterinary Products Committee and Veterinary Residues Committee, and works alongside other official bodies such as the Food Standards Agency and the Environment Agency (EA) or Scottish Environment Protection Agency (SEPA).

NOAH supports scientific approval and works to ensure regulatory controls are managed in such a way as to protect human and animal health and the environment while encouraging investment in the animal medicines of the future.

NOAH promotes self-regulation by the animal health industry in matters relating to product promotion. The Code of Practice for the Promotion of Animal Medicines ensures ethical standards are upheld when animal medicine companies market their products. Its purpose is to ensure that marketing information is fair, accurate and objective.

The code is upheld by the NOAH Code of Practice Committee, which is chaired by an independent practising barrister, has an independent secretary and includes representatives from both the farming and veterinary professions. The code is regularly reviewed and updated and incorporates the European Industry Code of Practice.

NOAH also requires that its member companies’ representatives are AMTRA qualified. AMTRA, the Animal Medicines Training Regulatory Authority, is an independent, officially recognised regulatory body whose task is to ensure that the marketing, distribution, storage and handling of animal medicines in the UK is undertaken in a responsible manner. This is achieved through examination syllabus and training schemes.

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