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Information about the EU Regulations and their implementation in Northern Ireland
Order a certificate of free sale to export medical devices outside the UK.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
Engage with the Ministry of Defence (MOD) on SKYNET Enduring Capability (SKEC), the next generation of solutions for future satellite communication programmes.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Guidance for manufacturers, importers and distributors.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Advice on writing clear notices and maximising replies to your FSNs.
Information and guidance on a range of medical devices for users and patients.
How the supply of medical devices from Great Britain into Northern Ireland works.
Get help classifying computers, inkjet and toner cartridges and their components.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Find out how you could be made liable for the unpaid VAT of another VAT-registered business when you buy or sell specified goods.
How to use a quasi-experimental study to evaluate your digital health product.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
How to use an interrupted time series to evaluate your digital health product.
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