The European Mobile Laboratory, EMLab, was the first EBOV diagnostics unit deployed to the outbreak epicentre by WHO in March 2014.

14th June 2016 • comment

New articles from the African Society for Laboratory Medicine (ASLM).

13th November 2015 • comment
5th August 2015 • comment

In celebration of Global Health Trials' fifth birthday (May 11th 2015) Professor Trudie Lang, Principal Investigator of the programme, talks to us about why Global Health Trials was started, why people should share their experience, and what the future holds.

8th May 2015 • comment
2nd February 2015 • comment

Ebola PPE guidelines - urgent need to revise WHO and CDC guidelines. This video shows an excerpt from keynote address 'The fuss about face masks', Professor Raina MacIntyre from the School of Public Health and Community Medicine, UNSW Australia.

14th October 2014 • comment
28th March 2014 • comment
25th February 2014 • comment

The authors present the story of building a succesful research laboratory in Cameroon, including how they managed building up the infrastructure, equipment maintenance, staff training.

10th July 2013 • comment

In determining the feasibility of establishing a biorepository at your facility, there are several key factors to consider. But first, there are a few that must be in place before commencing. They are:

  • The commitment of your institutional
  • The trust of the community within which you work
  • Informed consents that allow specimens to be used for multiple research studies
  • Vision/commitment for the distribution and sharing of biospecimens and data with the wider scientific community
We attach here the facility checklist for biospecimen collection and storage, organized by topic, along with the relevant Best Practices from ISBER, for assessing the readiness your facility. The purpose of these checklists are to 1) identify any potential barriers to setting up long-term storage of biospecimens on site; and 2) enable you to take action, as needed.

8th January 2013 • comment

Laboratory data is crucial in ensuring subject safety and determining the effectiveness of an investigational medicinal product. Here are some issues to consider for clinical trial laboratories in resource-poor settings.

21st November 2009 • comment

The effort invested in pre-trial planning and preparation more than pays off in terms of smooth operations, happy staff, happy participants, good recruitment and ultimately high quality data.

21st November 2009 • comment