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

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

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.

Evaluation of Biobanks

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

EC and Biobank

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

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