Your data on MRCVSonline
The nature of the services provided by Vision Media means that we might obtain certain information about you.
Please read our Data Protection and Privacy Policy for details.

In addition, (with your consent) some parts of our website may store a 'cookie' in your browser for the purposes of
functionality or performance monitoring.
Click here to manage your settings.
If you would like to forward this story on to a friend, simply fill in the form below and click send.

Your friend's email:
Your email:
Your name:
 
 
Send Cancel

Colistin use in animals to be reviewed
pig
EMA says it will review its 2013 guidance, particularly relating to the use of colistin in pigs.
EMA asked to update its advice after MCR-1 discovery
 
The European Medicines Agency (EMA) may change its advice on the use of colistin in animals. The move follows the recent discovery of a gene called MCR-1 that causes bacteria to become resistant to this 'last resort' antibiotic.

MCR-1 was first detected in bacteria isolated from pigs, pork and chicken products, as well as a small number of humans in China. Since then, it has also been found in the EU.

Colistin is one of the last defence antibiotics used for treating humans with infections caused by multi drug resistant bacteria.

In light of the findings, the European Commission has asked the EMA to update its advice on the responsible use of colistin in animals.

Due to the drug's importance as a last defence against antibiotic resistant infections in people, the agency says it will review its 2013 guidance, particularly relating to the use of colistin in pigs.

The current advice recommends maintaining the use of colistin in veterinary medicine, but only for treating infected animals and those in contact with them, not preventative use.

It also said the surveillance systems for antimicrobial resistance should be strengthened, and a new review carried out if a substantial increase in resistance was identified in animal bacteria.

EMA has reconvened its Antimicrobial Advice Ad Hoc Expert Group to assess all the available information and decide whether the 2013 advice should be amended. The agency says any update will take into account the drug's importance to both human and veterinary medicine, the impact of resistance and the availability of alternative treatments.

Become a member or log in to add this story to your CPD history

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. 

Click here for more...
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.