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Register to vote Register by 18 June to vote in the General Election on 4 July.
Public list of companies in the UK who have had their licence/registration to manufacture or wholesale medicines/ingredients revoked or suspended.
The Chancellor has today (4 March) announced a significant investment package in the UK’s life sciences and manufacturing sectors.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Advice on writing clear notices and maximising replies to your FSNs.
If pharmacies wish to ‘pack down’ larger packs of a medicinal product, they need to follow these instructions
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
List of sites granted a manufacturer or wholesale dealer licence
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Documents related to the programme that aims to change young people’s perception of manufacturing.
What you need to know about and do to comply with the law and keep consumers safe.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Producer responsibility laws in the UK cover packaging, electrical and electronic equipment (EEE), batteries and end of life vehicles (ELVs).
Register as a manufacturer, importer or distributor of active substances.
Forms to make a variation to a manufacturer's licence.
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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