
Genetic Alliance UK’s new policy report – Time to Decide: Learning from international approaches to newborn screening decision-making
The report explores how the UK National Screening Committee can accelerate its approach to decision-making for expanding newborn screening, drawing on research findings from 14...

Public Genomics Café: Thursday 10 July, 11am, Microsoft Teams
Are you interested in finding out more about genomics and health, or affected by a rare or genetic condition? Join...

Sustainability of NHS at core of Wales Health Science Conference
The sustainability of the NHS was the focus of the recent Wales Health Science Conference 2025. The conference, which was...

Public Virtual Genomics Café: 22nd May 2025
Thursday 22nd May 2025 | 11:00 – 12:45pm | Microsoft Teams Are you interested in finding out more about genomics...

Genomics Partnership Wales Sounding Board Recruitment
Genomics Partnership Wales are committed to working with patients and members of the public, to explain things in a clear...

Young People’s Virtual Genomics Café | Thursday 27th February 2024 | 5:30-7:00pm | Zoom
Are you interested in finding out more about genomics and health, or affected by a rare or genetic condition? Join...

Public Virtual Genomics Café | Thursday 13th February 2025 | 11:00 – 12:45pm | Zoom
Are you interested in finding out more about genomics and health, or affected by a rare or genetic condition? Join...

Wales Gene Park at The Festival of Genomics & Biodata | 29-30 January 2025 | Excel, London
Join us in London on Wednesday 29th January – Thursday 30th January 2025 at the UK’s largest life sciences event...


Logo competition: Design a logo for the Digital Rare Care Centre!
Background The Rare Disease Implementation Network is working with Cardiff and Vale University Health Board to develop an all-Wales Digital...