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
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Regulators must use this process guidance note (PGN) to assess applications and write permits for paint application in vehicle manufacturing
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Regulators must use this process guidance note (PGN) to assess applications and write permits for mushroom substrate manufacturing.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Regulators must use this process guidance note (PGN) to assess applications and write permits for adhesive coating, including footwear manufacturing.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Regulators must use this process guidance note (PGN) to assess applications and write permits for pet food manufacturers.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
The rules that manufacturers and importers of fertilisers need to follow when trading in the UK.
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.