First Login to UK MVS - Quick Start Guide - Step 1

Ready to log in to the UK MVS?  Please follow the links to instructions below.

You will need your initial credentials issued by SecurMed:

  • Username and Password (you will be prompted to change your initial password the first time you log on to the UK MVS)
  • Software (TAN) Code – A short code which works in unison with the Username and Password to access the UK MVS

We have created videos to explain the processes for you.  By clicking on the Play button below, you can watch and listen before you begin.

STEP 1 - Download Certificate

  1. Click Certificate Portal url
  2. Log in using Username and Password
  3. Click on Certificate Download in the top menu
  4. Enter the TAN code where requested
  5. Click on Download Certificate
  6. Write down Passphrase provided in the Pop-up window
  7. Record your Passphrase in a safe place (if you need to download the certificate onto other hardware)

Need help?

If you are experiencing difficulties or require further support with your registration, please use the Contact Us form. 

These instructions are for PC users only. If you are  a MAC user, please read our Initial Production MVS Setup Guidelines for directions on how to continue.

Once STEP 1 is complete, go to STEP 2.

 

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Related articles

EU Exit and UK MVS

The United Kingdom formally departed from the European Union on 31st January 2020, entering into a Transition Period lasting until 31st December 2020.

Will Community/Hospital Pharmacies be able to return stock to their Wholesaler or a DTP manufacturer’s distributor?

This depends upon the terms and conditions of both the Wholesaler and the manufacturer. However, in general, we expect the current returns process will remain valid as long as the stock has not been decommissioned and the anti-tamper device is still intact.

Should we contact SecurMed to infiliate to GS1?

No. Please contact GS1 directly.

Does Article 37(d) require that a National Medicine Verification Organisation (NMVO) directly alerts the relevant national competent authorities, the EMA and the Commission about a falsification? Is there is a time limit for such alerting?

The use of the term “provide for” in Article 37(d) of Commission Delegated Regulation (EU) 2016/161 means that an NMVO has to ensure that the National Competent Authorities (NCA), the EMA and the Commission are informed.

Is Gibraltar in scope of the FMD implementation and what about British Crown Dependencies and British Overseas Territories?

MHRA have confirmed with the UK Foreign Office that the Crown Dependencies of Jersey and Guernsey (including the other Channel Islands) and the Isle of Man are included within the FMD implementation. Gibraltar and all other British Overseas Territories e. g.

Where can I find a copy of the Delegated Regulation?

You can find the Delegated Regulation here.

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