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Advice for medical professionals to follow when assessing drivers with neurological disorders.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
For manufacturers of long-term samplers and test laboratories who carry out testing of equipment.
Guidance for using automated grading techniques for beef carcase classification
How to conform with the legal requirements for placing medical devices on the market.
How to import or move live animals and germinal products from the EU to Great Britain.
Apply for premises approval to move animals covered by the Balai Directive.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
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