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Genetically modified salmon
Final stages of food safety approval for fish

Biologists in Canada are currently harvesting eggs from a genetically modified Atlantic salmon, which is in the final stages before being declared fit for human consumption.

The biologists, who work for a biotechnology firm, are going to keep the genetically modified fish – known as AquAdvantage salmon – in onshore tanks in Panama, Mexico.

They say the salmon will look just like their natural cousins, but will reach full-size in half the time. This improved growth is due to additional genes from the Pacific Chinook salmon and the ocean pout eel.

AquAdvantage salmon has already been declared to have "no significant impact" by the US food regulator, the Food and Drug Administration (FDA). This is normally the last step before official approval, however, there is still a brief period for objections.

The firm has been working on approval for AquAdvantage salmon for 17 years and, if given the green light by the FDA, the fish will be the first genetically modified animal fit for human consumption.

On the other hand, the Atlantic Salmon Federation fears that the fish, which are all female and sterile, could start breeding and disturb the ecosystem if they were to get into the wild.

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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.