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Read about the breakthroughs in biomedical science that are transforming the lives of the people and communities we serve.

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Showing 149 news posts

NIHR Exeter BRC-supported study advances fungal infection prevention in children

  • July 2nd 2026

Exeter joins new initiative to support clinical research careers in the UK

  • June 29th 2026

A “Copper Economy” helps fungi and bacteria build better biofilms

  • June 26th 2026

Large-scale population studies needed to reduce risks from newborn genome screening

  • June 16th 2026

Landmark UK Biobank epigenetics study will reveal impact of genes and environment on health

  • June 12th 2026

Exeter doctor wins international award for diabetes research

  • June 9th 2026

Genetic testing allows fast diagnosis of rare pancreatic condition in 98 per cent of babies

  • June 1st 2026

Exeter scientist elected to prestigious Academy of Medical Sciences Fellowship

  • May 21st 2026
An Exeter scientist has been elected to the Academy of Medical Sciences Fellowship, recognising outstanding contributions to medical research and scientific leadership.

Exeter researchers awarded £125,000 to lead national robotic hernia study

  • May 18th 2026
Exeter researchers have secured £125,000 to lead a national study investigating robotic surgery for hernia treatment and its impact on patient care and outcomes.

Mentoring initiative linked to NIHR Exeter BRC Clinical Mycology theme recognised in Wellcome report

  • May 14th 2026
A mentoring initiative connected to NIHR Exeter BRC’s Clinical Mycology theme has been recognised by Wellcome for its contribution to supporting research careers and culture.

Supporting health and care research in Cornwall with NIHR

  • May 12th 2026
NIHR partners in Cornwall are supporting the development of health and care research through collaboration, training and engagement with local communities and researchers.

Exeter leads rare disease global genetic testing project, improving access and saving young lives

  • May 6th 2026
Exeter researchers are leading an international project to improve access to genetic testing for rare diseases and support earlier diagnosis for children and families worldwide.

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