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Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
The government’s plan to support a thriving UK medtech sector and make sure the health and care system can reliably access safe, effective and innovative medical technologies to deliver the best outcomes for patients.
First published during the 2022 to 2024 Sunak Conservative government
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
First published during the 2019 to 2022 Johnson Conservative government
List of English speaking medical facilities for British nationals in Mexico.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Outlines the aim, scope and definitions of the medical technology innovation classification framework.
This notice advises what medical conditions are required to be reported on during the validity of an ENG1 medical certificate.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
List of Medical Facilities and Practitioners in Madagascar
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Employment Tribunal decision.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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