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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
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
An interpretation of the good manufacturing practice (GMP) requirements for specials manufacturers.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Advice on writing clear notices and maximising replies to your FSNs.
Documents related to the programme that aims to change young people’s perception of manufacturing.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
The MHRA register of licensed manufacturing sites - manufacturer specials (human) (MS) and manufacturer specials authorisation (veterinary) (MANSA) only.
What you need to know about and do to comply with the law and keep consumers safe.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Managing waste, health and safety, regulations
Estimates for UK manufacturers' sales by product (ProdCom) for 2021, including 2020 final sales data.
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