1. To improve the national collaboration regarding patients with IBD
2. To conduct 2-3 annual meetings in DCCD
3. A Scientific Committee has been founded in order to validate new proposals. Meetings are held four times annually
4. No one provides data without being inquired about the wish to participate in projects. Hereafter it is left to the Scientific Committee to decide the employment of the data
5. The Danish National Committee on Biomedical Research Ethics should approve all projects.