Within the legal distribution chain, the hospitals verify the safety features – the unique identifier and the anti-tempering device –  and decommission the unique identifier when supplying the medicine to the patient.

NOTE: Connecting your company/organization to the NMVS will be done through your software provider and through validation and registration procedures which fall under OSMR responsibility.

RECOMMENDATION: In order to connect to the National Medicines Verification System (NMVS), kindly ask the software providers to use the V5 version of the interface with the system. The V4 version will be disconnected within 2024.

Categories

 

ONBOARDING STEPS TO OSMR SIMI/NMVS

Steps that need to be followed  by the End-Users to onboard NMVS – IQE and PROD Environment

Examples of filling in the necessary documents for onboarding and for closing existing accounts in OSMR SIMI/NMVS

In oder to simplify the onboarding process or the closing of existing accounts in OSMR SIMI/NMVS, we have prepared two examples for filling in the necessary documents:

  • Onboarding of End-Users in NMVS – Participation Request, Terms and Conditions – Operational Phase, Self-Training Confirmation.
  • The Participation Request necessary for the Withdrawl/Closing of the existing account in OSMR SIMI/NMVS.
Inscriere in OSRM / Inchidere cont

 

Useful Documents for the End-Users’ Onboarding Process

Below you can find the End-User’s Onboarding Instruction Manual for the National Medicines Verification System (NMVS).

Inscriere in OSRM / Inchidere cont

Frequently Asked Questions and Answers – End-Users’ Registration

We have prepared a set of frequently asked questions and answers regarding the End-Users

Should you not find the answer to your question, please contact us.

FAQ Utilizatori Finali SNVM