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If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
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.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Forms to make a variation to a manufacturer's licence.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Register as a manufacturer, importer or distributor of active substances.
To apply for a manufacturer licence, complete the appropriate form. Applications for a manufacturer licence will be payable on invoice.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
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