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Check the tariff classification for various types of shelves suitable for use in the bathroom, shower or entrance hall.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
How to move and declare goods that have been imported or exported between the UK and the UK Continental Shelf.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Vegetables are nutrient dense and important sources of micronutrients but postharvest losses in sub-Saharan African range from 20 to 80%
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
How to apply to be an authorised treatment facility (ATF) for ELVs, comply with ELV regulations and meet recycling targets.
Find out which types of food are zero-rated and which are standard-rated for VAT purposes.
A company director and his pharmaceutical manufacturing company were sentenced in court today after pleading guilty to two charges of falsifying data that supported the shelf life of a medicine, adversely affecting its quality in order to obtain a licence...
This external quality assessment scheme is suitable for laboratories located on production sites where the introduction of pathogens may be inadvisable.
How to prepare for implementation and compliance of the Safety Features Regulation.
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