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Information about the EU Regulations and their implementation in Northern Ireland
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
Requirements for solid wood packaging used to import or export goods
What to do if you think you've spotted a scam pretending to be from Companies House, and examples of scam emails, letters and telephone calls.
Information and guidance on a range of medical devices for users and patients.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for manufacturers, importers and distributors.
How to get fast-track approval of medical devices during COVID-19.
A framework to help schools to collect information about their income and expenditure.
This page provides a collection of online media literacy resources and events.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Find the best guidance and tools to meet the accessibility regulations.
FCDO travel advice for the Dominican Republic. Includes safety and security, insurance, entry requirements and legal differences.
Data on the real-world efficacy of the COVID-19 vaccines.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Sources of radioactivity in the environment and how levels of radioactivity are monitored and assessed.
FCDO travel advice for Argentina. Includes safety and security, insurance, entry requirements and legal differences.
The Planning Inspectorate appeals casework portal - Terms and Conditions
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