Skip to content
  • About
    • What we do
    • Our history
    • Our team
    • Our committees
    • Our partners
    • About genomics
  • Services
    • What we offer
    • Research we’re supporting
  • Tools & resources
    • Search all tools & resources
    • Research ethics & governance
    • Consent & patient support materials
    • Evaluating genomic research & translation
    • Data governance
    • Access our datasets
    • Data capture & standardisation
    • Data analysis & interpretation
    • Workforce education
    • Projects actively recruiting
    • Our publications
    • Our submissions
  • Our project areas
    • Our project areas
    • Genomic implementation projects 2022-2024
    • Genomic information management
    • Clinical genomic practice
    • Genomic literacy, workforce & training
    • Indigenous genomic priorities
    • Genomic diagnostics
    • Evaluating genomic research & translation
    • Australian health system policy & practice
    • Involvement & engagement
  • News & events
    • News
    • Events
    • Personal stories
    • Search news & events
  • Connect with us

Genomics and genome editing in the NHS inquiry

Home All news & events News Genomics and genome editing in the NHS…

The UK Parliament’s Science and Technology Committee recently completed an examination of the UK Chief Medical Officer’s (Dame Sally Davies) call in her 2016 annual report, ‘Generation Genome’, for mainstreaming genomic medicine in the NHS within 5 years.

The Committee considered the conclusions from an interim report from the previous Committee on Genomics and gene-editing and sought submissions on observations of how any barriers to greater integration of genomic therapies in the NHS could be overcome.

The ‘Genomics and genome editing in the NHS’ Report of the inquiry, released on 20 April 2018, reported that the deployment of the UK’s world-leading genomics capabilities in the NHS is being held back by NHS digital infrastructure delays and reduced training budgets, and risks losing public support due to low public awareness of the benefits on offer. The report also calls for the Concordat and Moratorium agreed between the Government and the Association of 20 British Insurers, which prohibits insurers from basing premiums on predictive genetic information, be renewed.

The full report is available at here.