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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.

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Defra shares new Sanitary and Phytosanitary guidance

News Story 1
 Defra has published guidance for the vet sector ahead of a proposed UK-EU Sanitary and Phytosanitary agreement.

The agreement, which will change the movement and trade of animals and related products, could see reductions in checks, paperwork and certification. As well as describing regulatory developments, the advice highlights the importance of animal ID, registration and traceability in disease control and other compliance arrangements.

The guidance can be found here. More detail is expected as negotiations progress. 

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News Shorts
Lords Committee opens Pet Parasite Medication inquiry

The House of Lords Environment and Climate Change Committee will launch its inquiry into Pet Parasite Medication (PPM) on Wednesday (3 June).

Focusing on treatments containing fipronil and imidacloprid, the inquiry will seek to understand distribution pathways and the impacts of PPM use and non-use on biodiversity and human health. It will also cover current regulation, monitoring, and the potential implications for pets and their owners.

The committee will hear evidence from environmental non-governmental organisations and research institutes. The public can follow the proceedings live on Parliament TV or in person in the Palace of Westminster.