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.
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.
This template is intended to prepare an informed consent form (ICF) for adult patients participating in an interventional clinical trial.
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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
EC forms for evaluation of biobanks (last versions) developed by the BAREC workgroup on biobanks, in consultation with different stakeholders.
The BAREC workgroup on biobanks gave some more insights in the biannual evaluation of the biobanks during an online information session organised by BAREC and BBMRI.be
BAREC en BBMRI.be voorstellen tweejaarlijks rapport
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