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The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Foresight project looking at the long-term picture for the UK manufacturing sector between now and 2050.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
The Chancellor has today (4 March) announced a significant investment package in the UK’s life sciences and manufacturing sectors.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
The MHRA register of licensed manufacturing sites - manufacturer specials (human) (MS) and manufacturer specials authorisation (veterinary) (MANSA) only.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
The Medicines and Healthcare products Regulatory Agency (MHRA) has undertaken a further review of the safety of albumins manufactured from UK plasma with respect to vCJD.
The advanced manufacturing plan sets out the actions we are taking to be the best place in the world to start and grow a manufacturing business.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
How to import, export, or manufacture pre-charged equipment containing hydrofluorocarbons (HFCs) in Great Britain.
Keynote address delivered by the Minister for Industry and Economic Security at Make UK's National Manufacturing Conference.
Regulators must use this process guidance note (PGN) to assess applications and write permits for the manufacture of coating materials.
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