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Detailed guidance, regulations and rules
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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.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
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.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
The MHRA register of licensed manufacturing sites - manufacturer specials (human) (MS) and manufacturer specials authorisation (veterinary) (MANSA) only.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
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.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Documents related to the programme that aims to change young people’s perception of manufacturing.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Managing waste, health and safety, regulations
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Forms to make a variation to a manufacturer's licence.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Register as a manufacturer, importer or distributor of active substances.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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