Medical research involving human participants cannot take place without volunteers. If you have already been approached to take part in research, you can find information on the rights and obligations of participants under General information on taking part in research (IRP). This page forms part of the consent form that you sign before you taking part.
If you would like to know more about research and the possibilities to participate, you can also refer to the Background information on participating in research.
On the pages about the Patient Participation Program, you will find explanations about the ways in which the CCMO tries to better involve patients in the design and conduct of research.