TÜV Süd becomes second Notified Body designated to European MDR by NANDO.
At the same time, LQRA company announced it will no longer support CE Mark certification services under the current Medical Devices Directive (MDD) or In-Vitro Diagnostic Medical Device Directive (IVDD), and will not seek designation under the upcoming Medical Devices Directive (MDR) or In-Vitro Diagnostic Devices Regulation (IVDR). LRQA’s withdrawal of NB services is expected to be effective by September 10th, 2019.