NEWS
Establishing detailed rules for the safety elements which appear on the packaging of medicines for human use
The 1473 / 22.11.2018 Order of the Ministry of Health was published in Monitorul Oficial [...]
Updated Q&As Version – European Commission
An updated version of Questions & Answers has been released by the European Commission. We [...]
The Technical Solution in Use
Related to the technical solution in use, we kindly inform you regarding the use of [...]
Extension of the PILOT phase – January 15th, 2019
According to the European Medicines Verification System national implementation project Steering Committee decision taken on [...]
The first medicine pack scanned
The first medicine pack scanned in NMVS PROD environment On November 5th 2018, the scanning [...]
Letter to Stakeholders Regarding the Implementation of Safety Features Under the Falsified Medicines Directive 2011/62/UE
Letter to Stakeholders Regarding the Implementation of Safety Features Under the Falsified Medicines Directive 2011/62/UE [...]
The Romanian Organization for Serializing Medicines (OSMR) brings new specifications on the registration process for acces to the National Medicines Verification System (NMVS)
Marketing Authorization Holders (MAH), regardless of the physical location of the medicine packs which bear [...]
End Users’ direct request for NMVS access
Starting with October 15th, 2018, the legal entities that need to comply with the legal [...]
Publicare Proiect OMS privind normele metodologice de aplicare a Regulamentului Delegat 161/2016
Astazi, 28.09.2018, a fost publicat proiectul OMS privind normele metodologice de aplicare a Regulamentului Delegat [...]
MINIMUM TECHNICAL AND PROCEDURAL REQUIREMENTS FOR END-USERS
The End-Users registration process for NMVS access, according to the OSMR working procedures, is run [...]