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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information for health professionals on the epidemiology, transmission and prevention of Chlamydia abortus which can cause stillbirth or abortion in humans.
Official information British people moving to and living in the United States of America (USA) need to know, including residency, healthcare and driving.
How to use Method 2 to work out the customs value of your imported goods if you’re an importer or clearing agent.
Use form US-Individual 2002 to apply for relief at source or to claim repayment of UK Income Tax.
Bringing in goods for personal use when you travel to the UK from abroad - types of tax and duty, duty free, EU and non-EU arrivals, banned and restricted goods.
Ensuring you get what you pay for.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
How sellers deal with VAT for goods from overseas that they sell direct to customers in the UK.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
The controls that apply if you transport waste out of or into England.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
You may be able to pay no Customs Duty or a reduced amount of duty for goods you bring or receive into the UK, depending on what they are and what you do with them.
How to use a cost benefit analysis to evaluate your digital health product.
Pharmacovigilance system requirements
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