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SBV vaccine approved in France

Viremia prevented in infected sheep and cattle

A new vaccine against the schmallenberg virus (SBV) has been granted approval under exceptional circumstances in France.

The vaccine, named SBVvax, has been developed by animal health company Merial and will be available to veterinary surgeons in France by October.

During clinical studies, SBVvax was able to prevent viremia caused by SBV in 100 per cent of the infected lambs and calves tested. The vaccination protocol is one shot of 1ml for sheep and two shots of 1ml for cattle, three weeks apart.

SBV is a new virus that was first identified late 2011. It has since caused devastation to farmers across Europe, with more than 8,000 farms having confirmed cases over the past two years.

The vector-borne disease results in stillbirths, malformed newborns, low milk production and adult animal deaths, which largely impacts reproduction and productivity performance in herds.

Dr Silke Birlenback, head of veterinary public health at Merial, said: "When SBV arrived, we did everything we could to offer our customers a high-quality vaccine in record time.

"The first priority for us was to have a solution to protect herds, now we are looking forward to partnering with veterinarians, and the livestock and research community to enhance our understanding of this novel disease."

SBVvax is currently under review for the UK by the Veterinary Medicines Directorate (VMD). 

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FIVP launches CMA remedies survey

News Story 1
 FIVP has shared a survey, inviting those working in independent practice to share their views on the CMA's proposed remedies.

The Impact Assessment will help inform the group's response to the CMA, as it prepares to submit further evidence to the Inquiry Group. FIVP will also be attending a hearing in November.

Data will be anonymised and used solely for FIVP's response to the CMA. The survey will close on Friday, 31 October 2025. 

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News Shorts
CMA to host webinar exploring provisional decisions

The Competition and Markets Authority (CMA) is to host a webinar for veterinary professionals to explain the details of its provisional decisions, released on 15 October 2025.

The webinar will take place on Wednesday, 29 October 2025 from 1.00pm to 2.00pm.

Officials will discuss the changes which those in practice may need to make if the provisional remedies go ahead. They will also share what happens next with the investigation.

The CMA will be answering questions from the main parties of the investigation, as well as other questions submitted ahead of the webinar.

Attendees can register here before Wednesday, 29 October at 11am. Questions must be submitted before 10am on 27 October.

A recording of the webinar will be accessible after the event.