Work

D2.4 - Policy White Paper: Advancing Next-Generation Sequencing and Public Health Genomics in European Healthcare Systems

Year: 2025

Type: article

Abstract: This policy white paper, developed under the EU4Health-funded CAN.HEAL project (101080009), offers a strategic analysis of the integration of Next-Generation Sequencing (NGS) and Public Health Genomics (PHG) in European healthcare systems. Drawing from expert consensus and peer-reviewed research, the document identifies disparities in implementation across Europe, and outlines key policy, infrastructure, and data governance challenges. It provides actionable recommendations for EU and national policymakers, healthcare providers, researchers, and patient advocacy groups. The paper emphasizes the need for harmonized regulatory frameworks, workforce development, equitable access to genomic services, and cross-border data interoperability, positioning genomics as a cornerstone of future precision healthcare in Europe.

Source: Zenodo (CERN European Organization for Nuclear Research)

DOI: 10.5281/zenodo.15304424

Authors: Denis Horgan, Skarpa, Andela, De Las Heras Martin, Ane, Radovnikovic, Paola

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funder: European Commission

Award: G690532135