Safety Gate 2023

Draft standardisation request as regards medical devices and in vitro diagnostic medical devices

Draft standardisation request as regards medical devices in support of Regulation (EU) 2017/745 and in v...

Regolamento Delegato (UE) N. 392/2012 della Commissione del 1o marzo 2012 che integra la direttiva 2010/30/UE del Parlamento europeo e del Consiglio per quanto rig...

STEP 1 - Identify the directive(s) and harmonized standards applicable to the product

There are more than 20 directives setting out the product categories requiring ...