Yes, we are committed to providing all our customers with the same range of services post Brexit in the EU27 and the UK and we currently provide in the EU.
We are already approved as a Notified Body for the Lifts Directive in France by COFRAC: NoBo number 2748.
We have made applications for all other approvals in the Netherlands. LR intends to provide identical services to those currently provided through two existing Notified Bodies in the Netherlands, Lloyd's Register Verification BV (for Industrial Equipiment Directives and Transportable Container authorisations) and Lloyd's Register Nederland BV (for Medical Devices and In-Vitro Diagnostics Devices). Applications have also been made for Medical Devices Directives under 93/42/EEC and 98/79/EC to VWS/Directie GMT in the Netherlands for Notified Body approval for Lloyd's Register Nederland BV.
We have also made applications for ATEX, CPR, MD, MED, ND, PPE, PED and the SPVD directives to RvA in the Netherlands for NoBo approval for Lloyd's Register Verification BV. The applications are currently being assessed and we are expecting a firmer timeline to be available by mid July.
Additionally, we have prepared the required applications for TPED, ADR, and RID directives to De Inspectie Leefomgeving en Transport (ILT) in the Netherlands for NoBo approval.