Laboratory work

The purpose of the IBD BioResource is to foster important IBD research by any bona fide investigator whether from a university or from industry, particularly but not exclusively relating to the clinical translation of recent genetics advances. It should bring forward the possibilities of personalised medicine in IBD by providing access to large cohorts of patients who can be selected by genotype (all subjects will have GWAS data) or clinical phenotype. In short, we want to make high quality IBD research easier, so that current and future patients can benefit sooner!

Investigators can access the IBD BioResource by submitting a short application to outlining their proposed study, confirming its approval by a research ethics committee and detailing appropriate funding support.

Proposed studies may involve:
-Data access only
-Data and sample access
-Recall studies (for e.g. intervention studies, surveys and questionnaires, clinical trials)

The process to access the IBD BioResource panel is as follow:

Applications are considered by the NIHR BioResource Steering Committee/Scientific Advisory Board (SAB) and approval must be gained before the study can commence. Applications must be received by:

  • 9 September 2021
  • 4 November 2021

A maximum of 8 new applications will be considered at each NIHR BioResource Steering Committee meeting. Applications will go for feasibility checks, before being distributed to the Steering Committee for review; please allow 1 month from the dates shown above to receive feedback. If the next NIHR BioResource Steering Committee meeting is full or if your application is received after the deadline, it will be considered at the next available meeting.

Completed forms should be emailed to and

If your application to the SAB is successful you will be sent a Study Summary Template and Confirmation of Conduct form by our team to be completed. Volunteer recruitment will not commence until these forms have been returned to us. Please be aware that we may ask you to amend your study paperwork, including Patient Information Sheet and Consent Form, to ensure that it complies with our Protocol and standards before we are able to commence recruitment.

Patients meeting inclusion criteria will be contacted by the NIHR BioResource team with a letter of invitation and a patient information leaflet. For volunteers willing to participate appropriate arrangements will be made, for example, to gather information or collect fresh samples of blood or stool (this will be done by the NIHR BioResource team to preserve patient confidentiality), or perhaps engage patients in intervention studies (requiring clinical trials agreements to be set up with a subset of the hospitals participating with the IBD BioResource and then recruiting from their patient cohorts).

If you are interested in having your study supported by the NIHR BioResource please contact us at to have a discussion about your potential application- this can help your application, as we can check feasibility, or assist in necessary changes to your study ethics, before you submit an application.

The current cost guidelines for using the NIHR BioResource are outlined here

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