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“Risk-adverse” policies restrict progress of GM technology
Trial releases of GM insects for disease control are already happening in places such as the Caribbean, Malaysia and Brazil.
Regulatory frameworks and public concern affecting potential

Scientists from The Pirbright Institute have published a discussion paper addressing the restrictive components affecting the progress of GM technology in tackling global disease.

Dr Anusha Panjwani and Dr Anthony Wilson argue in their opinion piece, published in PLOS Pathogens, that more transparency is required in international regulation to increase trust in the companies developing new technologies.  

Amidst growing fears about insect-borne disease outbreaks and the environmental impact of current pest control, regional inconsistencies regarding the assessment of both risk and benefit are impacting the potential for solutions to come from GM technology.

The authors cite inconsistencies between countries as responsible for uncertainty and public concern about developing GM solutions.

Dr Wilson said: “Trial releases of GM insects for disease control are already happening in places such as the Caribbean, Malaysia and Brazil, but in other parts of the world, such as Europe, significant regulatory obstacles still exist well over ten years after the technology first appeared.

The paper addresses the current concern over public opinion. For example, GM crops facing high profile protests in the UK and Germany are readily supported in other countries such as the US and Brazil.The paper attributed public resistance to big companies monopolising the industry.

“Engagement with the public on this issue is not just about dealing with a knowledge deficit, it is about building trust both in the safety of the technology in the longer term and in the system for assessing and developing it”, said Dr Panjwani.  

In an attempt to address the current hindering attitude discrepancies surrounding GM technologies, the scientists propose solidifying greater transparency and broader involvement in the industry with a patent or embargo system to protect intellectual property.  

Pajwani and Wilson propose building trust in the safety of GM technology by standardizing the system for assessing and developing it.

Dr Wilson added, “The current regulatory system is hampering our ability to fight diseases which kill millions of people every year. Policy makers should therefore consider not only the risks - but the risks of the status quo as well.”

 

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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.