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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Guides councils in how to assess their housing needs.
How to use a quasi-experimental study to evaluate your digital health product.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
Hand luggage restrictions at UK airports - carry-on luggage, checked-in baggage, restricted items and liquids, electronic devices carried from Turkey, Lebanon, Egypt and Saudi Arabia
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to find digital outcome, specialist and user research services on the Digital Outcomes and Specialists framework.
FCDO travel advice for USA. Includes safety and security, insurance, entry requirements and legal differences.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
You need the right licence to drive a tractor or specialist vehicle, there are also age limits and specific rules for driving tests
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Find out what trade barriers are and how they may affect you when exporting goods or services.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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