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How to use a crossover randomised controlled trial to evaluate your digital health product.
This guidance explains the different preference tiers under the DCTS, including benefits for each tier, criteria for moving between tiers and transition periods.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
Apply for a High Potential Individual (HPI) visa if you've been awarded a qualification by an eligible university in the last 5 years - eligibility, fees, documents, switch, bring your partner and children
How to use a quasi-experimental study to evaluate your digital health product.
Integration is about ensuring Defence can act in a way greater than the sum of its parts, with government, our allies and industry to deliver a desired outcome.
Advice on planning for the housing needs of different groups.
This guidance explains our competition process and how your proposal is assessed.
The European Trade Mark and Design Network has produced a common practice for use when assessing the inherent distinctiveness of figurative trade marks containing descriptive and/or non-distinctive words.
How to use a factorial randomised controlled trial to evaluate your digital health product.
Guidance for businesses holding registered Community designs and international trade marks and designs.
Extradition processes and agreements between the UK and other countries, role of the Secretary of State, High Court and Supreme Court.
How to use focus groups to evaluate your digital health product.
Sections (2.01 - 2.41) last updated January 2024.
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