Useful Links

Useful Links

National Competent Authorities

GOV.UK guidance on:

To register for the FMD Safety Features newsletter, or for any queries about the FMD, please contact the Medicines and Healthcare products Regulatory Agency (MHRA).

Tailored guidance

Community Pharmacy

FMD Source

Hospital Pharmacy

NHS Specialist Pharmacy Service



Manufacturers Parallel Distributors and MAHs







SecurMed MAH

 Software Suppliers


SWS (Arvato Developers Toolkit)


European Medicines Verification Organisation (EMVO)

For more information, please visit the EMVO website, read the Annex I and Annex II Delegated Regulation or visit the European Commission website.

Live status of all of the Solidsoft Reply Countries

Related articles

Bulk Registrations: Will each Location have unique credentials?

Bulk Registrations are suitable for multiple organisations/companies within the same legal entity at the same time. Each organisation/company will be an individual End User Location and will therefore have its own Username and UKNI MVS Certificate.

Register as an End User

To register, please read our guidance below and the End User Licence Agreement (EULA) carefully. For more detailed information, please see our End User Registration Process Overview.

EU Exit and UK MVS

The United Kingdom Transition Period ended on 31st December 2020 and the UK became a third country in relation to the EU.

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.

Where can I find a copy of the Delegated Regulation?

You can find the Delegated Regulation here.