ICF template interventional trials adult patients
This template was developed by a dedicated working group coordinated by the CT-college.
This Informed Consent Form (ICF) template for interventional clinical trials with an investigational medicinal product (IMP) on adult patients was prepared by a dedicated working group. This working group consisted of representatives of BAREC (Belgian Association of Research Ethics Committees), pharma.be (the Belgian association of the innovative (bio)pharmaceutical industry) and patient organizations, and was coordinated by the CT-College.
If you would like to read more about this, please consider becoming a Barec-member and acquire access to our member area.
Please contact us for more information on becoming a member via: info@barec.be
