We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Managing waste, health and safety, regulations
Guidance to help applicants and licence holders get and maintain a manufacturer licence - MHRA guidance note 5.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
The MHRA register of licensed manufacturing sites: manufacturer specials - human (MS) and manufacturer specials authorisation - veterinary (MANSA) only.
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.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Register a new manufacturer's mark and access lists of approved and inactive measuring container bottles (MCB) marks.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
List of sites granted a manufacturer or wholesale dealer licence
Advice on writing clear notices and maximising replies to your FSNs.
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.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).