The introduction of an electric or electronic product on the European market requires that this meets the conditions of specific directives according to the use that the manufacturer intended.
Some of the main include the low-voltage directive (Directive2006/95 LVD) and Medical Devices Regulation 2017/745, which replaces the medical products Directive (Directive 93/42 MDD)
The tests that can be carried out by our partner laboratories include: