Guide for policy makers
You represent a ministry or public body backing the Genome EDIC. You want to know what the system delivers, what your country must provide, and whether it respects the commitments of the 1+MG Declaration.
Your questions and where to find the answers
| Question | Answer |
|---|---|
| What is the system for, and which uses does it support? | 1. Introduction and goals |
| What must my country put in place (organisation, infrastructure, people)? | 2.3 Organisational constraints |
| What stays under national control, and what is done at European level? | 3.3 European, national and User Organisation scopes |
| Who decides on access to which data: my country or the Genome EDIC? | 3.3 Scopes, ADR-0002 Who decides on access, per type of dataset |
| Do genomic data leave my country? | 4. Solution strategy |
| How does this fit the European Health Data Space (EHDS)? | 8.11 EHDS integration |
| Which options does my country have to organise its national node? | 7.2 National deployment patterns |
| What are the main risks and open issues? | 11. Risks and technical debt |
| Which key decisions were taken, and why? | 9. Architecture decisions |
| How is my country’s implementation described? | National implementation profile (template) |
tip
The box at the top of every page shows which governance sections the page implements. The governance traceability page shows, for every governance section, where it is implemented and what is still missing.