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Government confirms maximum transition period for zinc oxide
Piglets
Medicines containing zinc oxide are used in piglets for the prevention, or treatment and control, of diarrhoea.

Farmers have five years to find alternative strategy

The UK government has confirmed the maximum transition period of five years for zinc oxide to support the adoption of alternative management strategies.

The Veterinary Medicines Directorate (VMD) said that it strongly encourages the responsible use of medicines during this time.

‘The VMD recognises the challenge that the withdrawal presents and is committed to finding ways to assist with the transition,’ it said in a statement.
'We will invite representatives of the pig industry to meet with us in the coming weeks to discuss implementation of the Commission Decision.’

On 26 June, the EC adopted a decision to withdraw the marketing authorisations (MAs) for veterinary medicines containing zinc oxide administered by mouth to food-producing species. Member States now have up to five years to withdraw existing national MAs for these products.

In the UK, there are three veterinary medicines authorised for oral administration to food-producing animals that contain zinc oxide. These are used in piglets for the prevention, or treatment and control, of diarrhoea.

But late last year, the European Medicines Agency (EMA) Veterinary Committee concluded that zinc oxide in piglet feed should be withdrawn, as the benefits are outweighed by the risk to the environment and co-selection of antimicrobial resistance.

The VMD said there are a limited number of vaccines authorised within the EU for the prevention of diarrhoea in piglets. These are indicated for specific pathogens.

There are also a number of antibiotics that are authorised for treatment, or for prevention and treatment, of specific causes of diarrhoea in piglets. For more information, refer to the Product Information Database.

 

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Annual submission deadline small pet animal exemptions

News Story 1
 Companies marketing medicines for small pets exempt from authorisation must submit their annual return to the Veterinary Medicines Directorate (VMD) by 30 November 2026.

Submitting this annual return ensures continued compliance with regulatory requirements for products marketed without a full Marketing Authorisation. The exemption specifically applies to products intended for animals, cage birds, terrarium animals, small rodents, ferrets and rabbits.

For further details and submission guidelines, visit the gov.uk website.  

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BVA urges 'continued vigilance' over bluetongue

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In a recent statement, the BVA noted that members are reporting more severe clinical signs and higher mortality rates than in previous years.

'We know that farm vets are working hard to support farmers and animals affected by this outbreak, during what is an extremely difficult time for all involved,' they stated. 'Continued vigilance to identify disease early is vital and vaccination remains the best way of protecting animals from this disease.'