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Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Get a vehicle approved, register a vehicle, manufacturing regulations
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Check when packaging is classified as a finished plastic packaging component, and what is meant by substantial modifications, to find out if you must register for the tax.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
Foresight project looking at the long-term picture for the UK manufacturing sector between now and 2050.
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
Documents related to the programme that aims to change young people’s perception of manufacturing.
Guidance for manufacturers, importers and distributors.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
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