Overview
Screen4Care offers an innovative research approach to accelerate rare disease diagnosis based on genetic newborn screening and digital technologies. The project involves participation in genetic newborn screening and aims to shorten the path to rare disease diagnosis.
In the news
- Great to be part of the Innovative Health Initiative (IHI) Forum 2026 in Brussels! It’s inspiring to connect with so many experts from across academia, industry, healthcare, patient organisations, regulatory authorities, HTA bodies, and European institutions ✨ Bringing together such diverse perspectives highlights the importance of considering the entire pathway from #research to #impact, including how to facilitate the adoption of innovative solutions across diverse healthcare systems. We’re also delighted to have the
- The potential of NBS doesn’t end with screening. As we wrap up our #NewbornScreeningAwarenessMonth series, Vinciane Pirard from Sanofi reflects on how new technologies could help reshape the way we think about health, treatment and care 👇 #Screen4Care #RareDiseases #NBS
- Across Europe, there is still a long way to go towards equitable access to early diagnosis. Gulcin Gumus from EURORDIS-Rare Diseases Europe Europe shares her perspective on how genetic NBS could help change that. 👇 #NewbornScreeningAwarenessMonth #NewbornScreening #Screen4Care #RareDiseases
- How can NBS enable earlier intervention while ensuring its benefits are responsibly balanced? For Jan Kirschner from Universitätsklinikum Freiburg, realising the potential of NBS also means carefully considering the challenges it brings. 👇 #NewbornScreeningAwarenessMonth #NewbornScreening #Screen4Care #RareDiseases
- What role could NBS play in shaping the future of genomic medicine? For Alessandra Ferlini, Screen4Care Scientific Coordinator from Università degli Studi di Ferrara, the potential goes far beyond diagnosis 👇 #NewbornScreeningAwarenessMonth #NewbornScreening #Screen4Care #RareDiseases
- It’s September, which for us means one thing: Newborn Screening (NBS) Awareness Month is here! Throughout the month, we’ll be sharing voices from across the #Screen4Care team on where NBS stands today and where it could take us next. As a project committed to advancing NBS, raising awareness remains an important part of our mission, and we hope you’ll join the conversation. So make sure to follow along and stay tuned ✨ #RareDiseases #NewbornScreening
- Today, we join the global community in celebrating the International Day of Neonatal Screening! As a project committed to helping shape the future of #NewbornScreening, we are proud of the progress made together with our partners across Europe to enable faster diagnosis of rare diseases. We also celebrate the many projects, initiatives, and colleagues around the world who share this mission and are helping advance neonatal screening every day. 💙 Together, we are many. Together, we are building a future where every child has the
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