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How we are going to deliver our mission to grow the UK economy by providing an IP system that encourages investment in creativity and innovation.
Get help to classify textiles and which headings and codes to use.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How to use a quasi-experimental study to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
How the UK supports the use of combined heat and power (CHP) or 'cogeneration', which avoids network losses and reduces emissions.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
The UK government's design principles and examples of how they've been used.
Self-build and custom housebuilding registers.
All essential shared data assets (ESDA) must be assessed for data quality issues, made findable and be available through APIs.
How to use a case-control study to evaluate your digital health product.
How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Employment Appeal Tribunal Judgment of Judge Tayler on 30 April 2024.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
How to use a cost utility analysis to evaluate your digital health product.
How to conform with the legal requirements for placing medical devices on the market.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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