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Public list of companies in the UK who have had their licence/registration to manufacture or wholesale medicines/ingredients revoked or suspended.
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
The Chancellor has today (4 March) announced a significant investment package in the UK’s life sciences and manufacturing sectors.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Documents related to the programme that aims to change young people’s perception of manufacturing.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
Register as a manufacturer, importer or distributor of active substances.
Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
What you need to know about and do to comply with the law and keep consumers safe.
List of sites granted a manufacturer or wholesale dealer licence
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
The rules that manufacturers and importers of fertilisers need to follow when trading in the UK.
Estimates for UK manufacturers' sales by product (ProdCom) for 2021, including 2020 final sales data.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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