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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
This guidance provides an overview of the different tariffs for products exported to the UK under the DCTS, including how to identify commodity codes.
How to use a crossover randomised controlled trial to evaluate your digital health product.
How to tax a beneficial loan arrangement for a director or employee.
This guidance relates to the legal criteria for determining whether a building is considered a higher-risk building under the Building Safety Act 2022 and the Higher-Risk Buildings (Descriptions and Supplementary Provisions) Regulations 2023. It relates to the definition of higher-risk...
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Guidance on how to do detailed air quality modelling for specified generators.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
How the Northern Ireland Protocol affects supplementary protection certificates (SPCs), and what it means you need to do when applying for an SPC and afterwards.
Get help classifying computers, inkjet and toner cartridges and their components.
Standardisation explained.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
This page provides information on the outputs and outcomes definitions for the UK Shared Prosperity Fund.
How to create a model of how your digital health product works and choose measures for your evaluation.
How to set what you’ll evaluate digital outcomes, digital specialists, user research participants and studio suppliers on.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
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