{"id":876,"date":"2020-02-17T14:59:26","date_gmt":"2020-02-17T14:59:26","guid":{"rendered":"https:\/\/newsite.osmr.ro\/?page_id=876"},"modified":"2025-10-01T08:39:40","modified_gmt":"2025-10-01T08:39:40","slug":"home","status":"publish","type":"page","link":"https:\/\/osmr.ro\/en\/","title":{"rendered":"OSMR.ro"},"content":{"rendered":"

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The Romanian Medicines Serialisation Organisation<\/h2><\/div>

It ensures the implementation of Directive 2011\/62\/EU (FMD) and of the Delegated Regulation 2016\/161 (EU) of the European Commission so as to prevent the entry into the legal European supply chain of falsified medicinal products.<\/span><\/p>\n<\/div><\/div><\/div>

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OSMR<\/h1><\/div>
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<\/span> Medicines' Serialization<\/span>Medicines Alerts<\/span>Safe access to non-falsified medicines<\/span>Ensuring patient's safety through medicine's safety<\/span><\/span><\/span> <\/span><\/h4><\/div>
<\/i>About OSMR<\/span><\/a><\/div><\/div><\/div>\n

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NMVS Availability \u2192 <\/a>\u00a0<\/strong>
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The Romanian Medicines Serialisation Organisation<\/h2><\/div>

It ensures the implementation of Directive 2011\/62\/EU (FMD) and of the Delegated Regulation 2016\/161 (EU) of the European Commission so as to prevent the entry into the legal European supply chain of falsified medicinal products.<\/p>\n<\/div>

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About OSMR<\/span><\/a><\/div><\/div><\/div><\/div><\/div><\/p>\n
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Who is OSMR?<\/h2><\/div>
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The Romanian Medicines Serialisation Organisation (OSMR) is a non-governmental, autonomous, independent, apolitical and non-profit organization, established for the implementation of the European Directive no. 2011\/62\/EU of June 8th on falsified medicines and the Delegated Regulation 2016\/161.
\nOSMR is responsible for implementing and managing the National Medicines Verification System (NMVS), a verification platform through which pharmacies or other stakeholders, such as wholesalers in Romania, can verify the authenticity of a product.<\/p>\n<\/div><\/div><\/div>

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To whom it is addressed to:<\/p>\n<\/div>

End Users<\/h2><\/div>
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Pharmacies<\/h3><\/div>

Verify the safety features and decommission the unique identifier when supplying the medicine to the patient.<\/p>\n<\/div><\/div><\/div>

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Hospitals<\/h3><\/div>

Verify the safety features and decommission the unique identifier when supplying the medicine to the patient<\/p>\n<\/div><\/div><\/div>

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Wholesalers<\/h3><\/div>

Verify the authenticity of the unique identifiers of medicines\u2019 packs.<\/p>\n<\/div><\/div><\/div>

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Parallel Import Authorization Holders<\/h3><\/div>

Verify the authenticity of the unique identifiers of medicines\u2019 packs.<\/p>\n<\/div><\/div><\/div><\/div><\/div><\/div><\/div><\/div>

Marketing Authorization Holders & Parallel Import Authorization Holders<\/p>\n<\/div>

MAH & PIAH<\/h2><\/div>

The Marketing Authorization Holders and the Parallel Import Authorization Holders connect to the European Hub via the OBP (On-Boarding Partner) and ensure that the information related to medicines with unique identifiers is uploaded to the European Hub.<\/p>\n<\/div>

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Connecting to the NMVS<\/p>\n<\/div>

Software Providers<\/h3><\/div>

The registration process for access to the documentation and support for connecting your clients to the National Medicines Verification System is done by your company by going through the detailed procedure found on Arvato\u2019s site (NMVS solution provider)<\/p>\n<\/div>

Software Providers Registration<\/span><\/a><\/div><\/div><\/div><\/div><\/div>

Articles and News<\/h3><\/div>
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August 2026<\/h3>
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