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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.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Find out how to move a specific type of goods across the UK border - including licences and certificates, calculating tax and duty, and making declarations.
Getting a UK background check so you can apply for Global Entry and get through USA border control faster: how to apply, how much it costs
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
Learn how to check if your website or mobile app is accessible.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Using an ecological momentary assessment to evaluate your digital health product.
Guidance on the many ways for suppliers to work with the Defence Science and Technology Laboratory (Dstl), the science inside UK defence and security.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Find out about the ways people can make certain decisions for you or do certain things on your behalf
Compare different evaluation approaches and choose an appropriate method.
Find out how the ATA Carnet works, what to do at customs, and what happens if your goods are lost, destroyed or stolen.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to use an ethnographic study to evaluate your digital health product.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
Check recent contacts from HMRC to help you decide if a suspicious email, phone call, text or letter could be a scam.
How to use a quasi-experimental study to evaluate your digital health product.
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