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Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Information on using the app when applying to work, study or live in the UK.
Information for EU citizens and their families applying to the EU Settlement Scheme.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Where to scan your ID document if applying for EU Settlement Scheme (settled status) and you do not have access to an Android phone, or an iPhone 7 or above.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
SAPIENT enables interoperability of artificial intelligence (AI) enabled sensors, combined with intelligent fusion and sensor management.
We’re working to help people securely prove who they are without having to rely on physical documents.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
You might need to create a new Government Gateway account if you have forgotten both your user ID and password.
Guidance on the 2011 cancellation of identity cards, and information about new suppliers working with the Identity and Passport Service.
Application form ID2: certificate of identity for a corporate body.
Information and guidance for verifying your identity.
Application form ID3 to prove your identity when lodging an application to HM Land Registry.
How to use the Trade Tariff tool or get help to classify your goods, so you pay the right amount of Customs Duty and import VAT.
Check the tariff classification for peptide nisin standardised with sodium chloride
Keep up to date with the UK policy development in respect of Standard Essential Patents.
Find out how to get an agent reference number for VAT, VAT Mini One Stop Shop (MOSS), NOVA or VAT EU Refunds for Agents.
Information on how to use a High Integrity Telecommunications System.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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