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Guidance issued to NHS medical directors
This advice has been written by the Plastic, Reconstructive and Aesthetic Surgery Expert Advisory Group (PRASEAG) at the request of the Medicines and Healthcare products Regulatory Agency (MHRA – UK regulator). It is in the form of questions, asked of...
This analysis relates to patients who have had mesh procedures for SUI and urogynaecological prolapse since 2008.
Guidance on decontamination and infection control, including surgical instruments, dental equipment, endoscopes and benchtop steam sterilizers.
How to use a case-control study to evaluate your digital health product.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
The goal of ESM-Ketamine is to support universal health coverage by increasing access to surgery for vulnerable populations
These guidelines set out how the IPO examines patent applications for medical inventions.
Advice for medical professionals to use when assessing drivers with cardiovascular disorders.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Guidance for healthcare professionals on infection control and clinical aspects of M. chimaera infection associated with cardiopulmonary bypass.
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Form to report patients meeting the case definition.
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