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How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
A glossary of terms used across Ofsted’s education inspection information and guidance.
List of words and phrases that will cause a veterinary product to be medicinal by presentation either through use or contextual use.
Get help to classify textiles and which headings and codes to use.
You’re disabled under the Equality Act 2010 if you have a physical or mental impairment that has a 'substantial' and 'long-term' negative effect on your ability to do daily activities
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
The characteristics, symptoms, diagnosis and epidemiology of chikungunya.
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