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Alerts’ Guide

poza alerte

Constant communication, openness and transparency with the project’s stakeholders have been set from the beginning as core elements in establishing a communication channel focused on sharing of qualitative information. Thus, driven by the willingness to provide more details on the entire process of alert handling and most importantly, to offer some recommendations for End-Users on […]

NMVS Maintenance Session – PROD Environment – 01.12.2022 & 07.12.2022

Maintenance

Please be informed that on 01.12.2022 and on 07.12.2022, between: 22:00 – 23:30, a maintenance session is scheduled on the Production (PROD) Environment of the National Medicines Verification System (NMVS). Within the specified time interval, NMVS may be unavailable for short periods of time.

To the attention of NMVS End-Users – Hospitals and Wholesalers

UF pic

Based on the legal provision of the Delegated Regulation 2016/161 Art 37 (b), Art 33 (2), OSMR periodically verifies the identity, role and legitimacy of the National Medicines Verification System’s (NMVS) End-Users, ensuring that only the End-Users whose data has been verified and is valid/correct can access the NMVS production environment (PROD). Thus, following the […]

EMVS Community Newsletter – October 2022

emvs nl

The October edition of the European Medicines Verification System – EMVS Newsletter has been published. This edition presents the perspective of the Romanian NCA (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale din Romania – ANMDMR) on serialization. Please click on the link below for more details: EMVS Community Newsletter

NMVS Release – Core 1.11

pic NMVS Core 1.10

Yesterday, October 24th, marked the new release of the National Medicines Verification System (NMVS) – Core 1.11. This new version of the NMVS introduces soft tunning of the current functionalities and, most importantly, of the security characteristics. The specificities of the new elements brought by the new release have been highlighted below: