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).
|Manufacturers Parallel Distributors and MAHs||
SWS (Arvato Developers Toolkit)
European Medicines Verification Organisation (EMVO)
Live status of all of the Solidsoft Reply Countries
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.
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.
The United Kingdom Transition Period ended on 31st December 2020 and the UK became a third country in relation to the EU.
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.
You can find the Delegated Regulation here.
Please consult the UK government website.