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Register to vote Register by 18 June to vote in the General Election on 4 July.
International regulations and required documentation for hauliers transporting dangerous or hazardous goods by road or by vehicles on ships.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Customs and security requirements for rail freight movements entering or leaving the UK.
Information about the EU Regulations and their implementation in Northern Ireland
The UK’s consumer connectable product security regime came into effect on 29 April 2024. Businesses in the supply chains of these products now need to be compliant with the legislation.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
Guides councils in how to assess their housing needs.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
How to find digital outcome, specialist and user research services on the Digital Outcomes and Specialists framework.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out what trade barriers are and how they may affect you when exporting goods or services.
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