In each country, NCDNs can be the go-to place:
- For Researchers, to look for tools and services to support their data management plan, data analysis, data archiving, and data reuse;
- For Data Holders, to look for EHDS-compliant data quality indicators, data standards, data models, and hands-on support;
- For people to work together on mutually interested topics, such as data sharing tools, common data models for clinical applications (e.g., molecular tumor board, multi-disciplinary team discussion), patient-level data linkage solutions, and more;
- For National Funders, to understand how EU-funded projects interact with key national stakeholders and vice versa;
- For Patients, to find evidence-backed information about cancer, share data, and share concerns in a safe community space, powered by the European Cancer Patient Digital Center (ECPDC);
- For Doctors and Healthcare Providers, to look for help in addressing issues during daily practice, such as gathering relevant data for decision-making, the molecular tumor board (MTB), and multidisciplinary discussions;
- For Policymakers, to ask questions to the right national players.
