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

Boehringer's classical swine fever live vaccine approved
CSF has caused huge economic losses to China's pig farming industry.
Vaccine will play a vital role in eradicating the disease in China.

The first classical swine fever (CSF) live vaccine, jointly developed by Boehringer Ingelheim and Chinese research institutes, has received marketing approval.

The newly-approved Ingelvac CSF MLV is set to provide China's swine industry with breakthrough immunization programmes and support disease solutions. It will also play a vital role in eradicating CSF in the country.

CSF is a highly contagious, lethal disease that has caused huge economic losses to China's pig farming industry. While the outbreak is now effectively controlled by mass vaccination with CSF live vaccine, endemic and sporadic spread remains.

Existing CSF live vaccines can only be stored at -15℃  for 18 months, with strict temperature control requires for transportation, storage and dilution. The new vaccine uses state-of-the-art suspension culture and freeze-drying technologies to ensure stable vaccine production process, and controllable quality. It can be stored at 2-8℃ for 24 months.

In a press release, a Boehringer spokesperson said the vaccine ' marks another milestone for Boehringer Ingelheim’s “in China, for China”, as the company is committed to providing innovative and high-quality swine vaccines for the Chinese swine industry, as well as holistic swine disease solutions to pig farms.'

Ingelvac® CSF MLV will be produced by Boehringer Ingelheim’s Taizhou plant and is expected to be commercialised in early 2021. 

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.