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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.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Get help to classify textiles and which headings and codes to use.
Get help classifying computers, inkjet and toner cartridges and their components.
How to use a quasi-experimental study to evaluate your digital health product.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance for suppliers and dealers.
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