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Get help to classify textiles and which headings and codes to use.
Guidance on the mammographic aspects (both clinical and technical) of breast screening QA and the quality control of radiographic procedures.
Guidance issued to NHS medical directors
The purpose of this committee was to assess existing arrangements for ensuring the quality and safety of cosmetic interventions.The committee's work has concluded. It published its final report in April 2013 that sets out recommendations to protect people who choose...
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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 requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
Product Recall for a breast care machine presenting a serious risk of electric shock.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
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