Screen4Care Co-Announces the Formation of the International Consortium on Newborn Sequencing (ICoNS)

Our project proudly joins the launch of the International Consortium on Newborn Sequencing (ICoNS), with the aim of aligning stakeholders and establishing guidelines based on empirical evidence for th...

Signalise Podcast: Screen4Care EFPIA Lead Nicolas Garnier in Conversation With Kimberly Thomas-Tague

In episode 22 of Signalise: a Dazzle4Rare Podcast, Dr. Nicolas Garnier, EFPIA Lead of Screen4Care, joins host Kimberly Thomas-Tague for an engaging discussion on newborn screening. The episode sheds...

Coming Together to Shorten the Path to Rare Disease Diagnosis – First Face-To-Face Meeting of the Screen4Care Partners Held in Ferrara, Italy

The location for the long-awaited first in-person Annual Meeting of Screen4Care could not have been more welcoming than the beautiful city of Ferrara, Italy. From March 6th to 7th, 36 project partners...

EU Knowledge Valorisation Week 2023: Learn More on Turning Research into Solutions

Join stakeholders and policymakers at the EU Knowledge Valorisation Week between 25 April and 28 April 2023. The annual event highlights best practices promoting the uptake of research results and sci...

New partner brings valuable expertise to the table: Biopharma company PTC Therapeutics joins Screen4Care

Accelerating rare disease diagnostics through genetic newborn screening and digital solutions.

Since launching in October 2021, Screen4Care is dedicated to shorten the diagnosis journey for people l...

Screen4Care workshop on legal, ethical and business-related issues in Bern

On 22 April, the members of Work Package 1 met in Bern to discuss legal, ethical and business-related issues. The workshop was held in hybrid form with online and offline groups in the new building...

EURORDIS' Rare Barometer Survey on the Journey to Diagnosis for People Living with a Rare Disease

Screen4Care’s key partner EURORDIS has launched the Rare Barometer survey – an international survey on the journey to diagnosis for people living with a rare disease. The survey is open to people...

New EU Research Project “Screen4Care”

Accelerating Diagnosis for Rare Disease Patients Through Genetic Newborn Screening and Artificial Intelligence

The international consortium aims to tackle the major hurdle for rare disease patients...