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Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
The CMU is part of the Medicine, Pharmacy and Industry Group of DHSC which looks at supply and procurement in hospitals.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Your rights and security searches, body scans and privacy rules if you're disabled or taking medication aboard aircraft
On 18 March the Defence Secretary announced new measures to enable armed forces personnel to support public services in response to the coronavirus outbreak.
Guidance for owners and masters about potentially hazardous medical supplies.
This paper analyses strengths and weaknesses of the public and private supply chains into the health sector
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance on sources of electromagnetic interference and mitigating the risks.
UK guidance on re-manufacturing of Single-use medical devices.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
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