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This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to use a micro-randomised trial to evaluate your digital health product.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Assessment framework specification files for software suppliers developing management information systems (MIS).
How to use a cost benefit analysis to evaluate your digital health product.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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