Consent form preparation involving patients

All regulatory documents required for sample collection, and in particular patient documents (consent and information leaflet), which will have been proofread by a committee of expert patients to ensure that they can be understood by the general public. These documents will ensure compliance with French and European laws on biomedical research. Patients will be involved in the writing and review of all regulatory documents required for sample collection, and in particular patient documents (consent and information leaflet) to ensure that they can be understood by the general public.