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ICF template for interventional clinical trials with trial medicine in HEALTHY adult participants

Written by Editor on . Posted in ICF.

This template is intended to prepare an informed consent form (ICF) for healthy adult participants taking part in an interventional clinical trial with a trial medicine.

NL_Model-ICF_Interv-trial_Healthy_Participants_version1_20250131Download
FR_Model-ICF_Interv-trial_Healthy_Participants_version1_20250131Download
EN_Model-ICF_Interv-trial_Healthy_Participants_version1_20250131Download
SponsorStatementModel_CTR_healthy participants_V2_20250206Download

ICF template for adult patients participating in a clinical investigation involving a medical device (MDR-studies)

Written by Editor on . Posted in ICF.

This template is intended to prepare an informed consent form (ICF) for adult patients participating in a clinical investigation with a medical device, that is assessed by an independent Belgian Ethics Committee recognized under the Belgian legislation of 7 May 2017.

NL_Model ICF_Clinical_Investigation_Adult_Patients_version2_1_20250520Download
EN_Model ICF_clinical investigation_Adult_Patients_version1_1_20250520Download
FR_Model ICF_Clinical_Investigation_Adult_Patients_version1_1_20250520Download
SponsorStatementModel_ICF_clinical investigation_adult_patients_V2_20250206Download
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