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Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
How to make sure your business’ terms and conditions are fair, and avoid unfair contract terms
Sets out changes in terminology in definitions relating to waste reporting obligations.
How to use a clinical audit to evaluate your digital health product.
This guidance has been designed to support public sector teams completing algorithmic transparency reports.
The terms of reference outline the objectives, scope, and methodology of the General Review which is expected to begin in 2024.
When applying to register a trade mark, you must use the classification system to specify the goods and/or services you'll be using it on.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Use these general provisions to help you determine the origin of your products.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
Find out about the ways people can make certain decisions for you or do certain things on your behalf
This project scoped the programme of research required to develop tools capable of modelling entire systems in order to answer important questions about flood risk.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How Union GEA authorisations permit the export of specified controlled dual-use goods from Northern Ireland to certain countries outside the EU.
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