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How to use a quasi-experimental study to evaluate your digital health product.
Blogs where government organisations talk about their work and share information and ideas.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
The laws on selling, buying and carrying a knife or weapon depend on the type of knife or weapon, your age and your circumstances.
Guidance for people with symptoms of a respiratory infection including COVID-19, or a positive test result for COVID-19.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
ARIA will focus on projects with potential to produce transformative technological change, or a paradigm shift in an area of science. ARIA is an executive non-departmental public body, sponsored by the Department for Science, Innovation and Technology .
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The Scientific Advisory Committee on the medical implications of less-lethal weapons (SACMILL) provides independent advice to UK government departments and organisations on the biophysical, biomechanical, pathological and clinical aspects of less-lethal weapon systems. SACMILL is an advisory non-departmental public body,...
Get help to classify drones and aircraft parts for import and export.
How to get fast-track approval of medical devices during COVID-19.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
The Committee on Mutagenicity of Chemicals in Food, Consumer Products and the Environment (COM) assesses and advises on mutagenic risks to humans. COM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care and the...
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Don’t include personal or financial information like your National Insurance number or credit card details.
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