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 periodic checks of the End-Users’ data, OSMR has found that for several End-Users accounts, the Sanitary Authorisations existing in CRM-SIMI (support system type CRM – Client Relationship Management with the purpose of ensuring the legal obligations under Art. 37 letter b) of the Delegated Regulation 2016/161 are met) have not been updated.

The End-User is fully responsible for the validity of the data underlying the registration, access and use of the NMVS and maintaining the accuracy of this data, obligation assumed by signing the Terms and Conditions document.

Hospital & Wholesalers End-Users are kindly asked to check the validity of the Sanitary Authorisations/Wholesale Distribution Certificate related to the Wholesale Distribution Authorisation available in CRM-SIMI and, for accounts with expired authorisations/certificates, to upload the latest version.