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Information about the EU Regulations and their implementation in Northern Ireland
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
This guidance is for UK Conformity Assessment Bodies (CABs) who are intending to subcontract tasks such as testing, certification or inspection.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Check which reservations are relevant to UK businesses selling services to customers in EU member states.
Guidance providing practical information for placing construction products on the GB market.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
Approval process for gas and electricity meters under GB national legislation.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
When you can use a designated UK-based conformity assessment body (CAB) to test your goods against the importing market’s regulations.
An overview of the changes made to the Railways (Interoperability) Regulations 2011 that came into force on 1 January 2021.
Form CON2: consent to an application for the freehold estate to cease to be registered as a freehold estate in commonhold land during the transitional period.
How to apply to become an authorised consignor or consignee, and get authorised for other transit simplifications.
Consumers and patient groups are invited to submit evidence of their experience
What you need to know about and do to comply with the law and keep consumers safe.
Statement of the government’s policy on conformity assessment and accreditation.
Transfer of engagements and amalgamations: guidance from the Certification Officer (CO).
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