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How you import from and export to Mexico.
We’re a unit located within core-Defra that supports Defra and the Scottish, Welsh and Northern Ireland governments and their paying agencies to administer the Common Agricultural Policy (CAP) in the UK in accordance with the UK’s Withdrawal Agreement with the...
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Find out about the help you can get in the UK and abroad, including from victim support and the local British embassy or consulate.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance on the many ways for suppliers to work with the Defence Science and Technology Laboratory (Dstl), the science inside UK defence and security.
The UK government's design principles and examples of how they've been used.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How you import from and export to Turkey.
This information is provided to help British nationals make decisions about getting medical advice and reporting a rape or sexual assault in Russia.
How to use a cost effectiveness analysis to evaluate your digital health product.
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
The British Museum (BM) was the first national public museum in the world. Its permanent collection, over 8 million works, is amongst the largest and most comprehensive in existence and originates from every continent, illustrating and documenting the story of...
How to use a case-control study to evaluate your digital health product.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
Your responsibilities as a public body when carrying out or approving works on or near sites of special scientific interest (SSSIs).
How investigators and sponsors should manage clinical trials during COVID-19
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