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How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Apply for a Temporary Work - Religious Worker visa to do religious work in the UK - getting sponsored, fees, eligibility, family members
How to access social care, and support if you, or someone you care for is blind.
Guidance for manufacturers, importers and distributors.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
IT managers should now be planning how to migrate their PSN services to the cloud.
This guide provides information about being arrested in Turkey and what conditions are like in prison there.
Check timescales for the Legal Aid Agency (LAA) to process your work (eg prior authority application, graduated fee claims).
Check the tariff classification for a clip-on camera lens attachment made of glass.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
Information about the EU Regulations and their implementation in Northern Ireland
Portland is a prison and young offender institution (YOI) on the Isle of Portland, Dorset, for men aged 18 and over.
New proposals to give consumers confidence to take up smart devices.
Find out about which goods and services for disabled people and people aged 60 or over that you should apply zero or reduced rate VAT.
To help developers of low carbon electricity projects make final investment decisions ahead of the Contract for Difference regime being put in place as part of Electricity Market Reform
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
From 1 October 2024, more materials facilities will need to sample and report their waste. Sampling and reporting will be more detailed and more frequent under the amended regulations.
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