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The authors of this review sought to identify every study where people with an abdominal injury were randomised to surgery or observation
We are seeking your views on what procedures should be in scope of the licensing scheme for non-surgical cosmetic procedures in England.
People and businesses are invited to share their views on how to make non-surgical cosmetic procedures safer as thousands complain of ‘botched’ procedures.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Section (4A.01 - 4A.31) last updated October 2023.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
How to use an N-of-1 study to evaluate your digital health product.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
How to apply for repayment of import duty and VAT on protective equipment or medical supplies brought into the UK from non-EU countries from 30 January 2020 up to 31 December 2020.
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