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Advice for manufacturers and retailers on textile labelling.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
This guidance explains what rules of origin (RoOs) are and the changes under the Developing Countries Trading Scheme (DCTS).
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Check the tariff classification for a sleeveless knitted garment (a so-called running vest).
Use this list to check if you can claim a fixed amount of tax relief (also known as 'flat rate expenses') for your work expenses if you're an employee.
This research is part of the Gender, Growth and Labour Markets in Low-Income Countries programme.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
This research is based on direct surveys of garment workers and interviews and focus-group discussions
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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