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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.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
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.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Guidance for manufacturers, importers and distributors.
The VMR sets out the statutory fees associated with various regulatory services provided by the VMD. The statutory fees and fee structure are implemented from 17 May 2024.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Advice on writing clear notices and maximising replies to your FSNs.
If pharmacies wish to ‘pack down’ larger packs of a medicinal product, they need to follow these instructions
List of sites granted a manufacturer or wholesale dealer licence
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
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