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BVA Welcomes EU Decision on Laboratory Animals
Professor Bill Reilly, President of the BVA
The BVA has welcomed the announcement of a new EU Directive aimed at reducing the number of animals used in laboratory experiments, tightening controls over such procedures and harmonising improved standards of care throughout Europe.

President of the BVA, Professor Bill Reilly said: “The UK already has a firm commitment to the principle of the Three Rs – replace refine, reduce – and the BVA is pleased that MEPs have voted to firmly anchor this principle in the new legislation so that the practice can be implemented across the EU. The BVA is also pleased that the new Directive requires all establishments within the EU to have a designated veterinarian with expertise in laboratory animal medicine, charged with advisory duties in relation to the well-being and treatment of the animals.
 
“The responsible use of animals in research has improved both human and animal welfare, but we believe animals should only be used where no non-animal alternative is available and the work is justified through independent ethical scrutiny.
 
“The BVA continues to support the principle of the Three Rs and is committed to advocating for a reduction in animal usage in the future.”
 

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Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

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News Shorts
New form for online veterinary medicines retailers

The Veterinary Medicines Directorate (VMD) has produced a new online form for retailers wishing to sell veterinary medicines on the internet.

The form replace the previous Word version and is part of the VMD's ongoing commitment to digitise its processes. Anyone retailing prescription medicines online, including POM-V, POM-VPS and NFA-VPS categories, is lawfully required to register with the VMD before trading.

The change only applies to new applicants. Retailers already listed on the VMD's Register of Online Retailers or registered under the Accredited Internet Retailer Scheme (AIRS) do not need to do anything.