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Official information British people moving to and living in the United States of America (USA) need to know, including residency, healthcare and driving.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to ensure the products you make or import comply with the law and are safe for consumers to use.
This guide is to help you and your business understand issues around data protection and privacy. It is intended for organisations that provide online services likely to be accessed by children.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
Information to help you identify if your organisation needs to publish a modern slavery statement and best practice guidance on producing a statement.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out your VAT obligations if you use an online marketplace to sell goods in the UK.
Your council must help if you’re legally homeless or will become homeless within 8 weeks. Help may include advice, emergency housing or longer-term housing.
The Planning Inspectorate appeals casework portal - Terms and Conditions
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Find out what to expect from a site visit carried out by an RPA field officer to check you’re complying with your SFI agreement.
Apply for an India Young Professionals Scheme visa to live and work in the UK if you're an Indian citizen aged 18 to 30 - eligibility, fees, documents.
Understand how preventative design measures can reduce the risk of harms happening on your online platform.
Sources of radioactivity in the environment and how levels of radioactivity are monitored and assessed.
How to conform with the legal requirements for placing medical devices on the market.
This guide explains what the public register is, what details you need to give us, and how the public can access this information.
Guidance and templates on how to complete a site condition report under Environmental permitting regulations (EPR).
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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