The European Commission has recently updated its list of the standard fees charged by EU Notified Bodies. The revised list includes the fees of Notified Bodies that have been designated since the previous publication, such as Malta Conformity Assessment (MCA).
The updated list provides manufacturers with a useful reference for comparing the standard fee structures of designated Notified Bodies across the European Union when planning conformity assessment activities under the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR).
The updated list can be accessed using the following link
