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

EMA launches consultation on development of TB medicines
Pills in a jar
Existing treatments for TB are not effective at combatting the disease.

Comments invited on draft guidance until 31 January 2017

A public consultation on revised guidance on the development of new medicines to treat tuberculosis (TB) has been launched by the European Medicines Agency (EMA).

The revised guidance takes into account a recent shift towards developing new regimes to treat TB, instead of focusing on single medicines.

Stakeholders can send their comments to the EMA until 31 January 2017 and, in November 2016, EMA will also host a workshop to discuss stakeholders' comments on the revised guidance. This will be broadcast live and comments will be taken into account in the finalisation of the guideline.

In 2014 there were approximately 340,000 new TB cases and 33,000 deaths, mostly from eastern and central European countries. Although the disease is slowly declining worldwide, the burden of TB is still high with around 1.5 million fatalities a year.

Existing treatments for TB are not effective at combatting the disease because they are lengthy, complex and generally show reduced efficacy against MDR-TB. They also impose a heavy burden on patients, families and healthcare systems.

The EMA say that new TB medicines and regimes that are simpler to administer, are of shorter duration, and can overcome drug resistance are 'urgently needed'.

Comments on the draft guidelines should be sent to idwpsecretariat@ema.europa.eu using this form.

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

Equine Disease Surveillance report released for Q4 2025

News Story 1
 The latest Equine Disease Surveillance report has been released, with details on equine disease from Q4 of 2025.

The report, produced by Equine Infectious Disease Surveillance, includes advice on rule changes for equine influenza vaccination.

Statistics and maps detail recent outbreaks of equine herpes virus, equine influenza, equine strangles and equine grass sickness. A series of laboratory reports provides data on virology, bacteriology, parasitology and toxicosis.

This issue also features a case study of orthoflavivus-associated neurological disease in a horse in the UK. 

Click here for more...
News Shorts
NSA webinar explores sheep tailing and castration

The National Sheep Association (NSA) is to host a free webinar on the castration and tail docking of lambs.

The webinar, 'Understanding the tailing and castration consultation: A guide for sheep farmers', will be hosted online on Monday, 2 March 2026 at 7.30pm.

It comes during a government consultation into the methods used for these procedures. Farmers are encouraged to engage before the consultation period closes on Monday, 9 March 2026.

The webinar offers clear and actionable guidance to support farmers to contribute meaningfully to the consultation and prepare for potential changes.

On the panel will be former SVS president Kate Hovers, farmer and vet Ann Van Eetvelt and SRUC professor in Animal Health and Veterinary Sciences Cathy Dwyer. Each panel member will utilise their own specialism and expertise to evaluate risks and outcomes to sheep farming.

Find out more about the webinar on the NSA website.