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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), (the Belgian association of the innovative (bio)pharmaceutical industry) and patient organizations, and was coordinated by the CT-College.


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