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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.
This guidance summarises the requirements, controls and sanctions that Border Force applies to firearms and offensive weapons when they are imported into the UK.
How to use chatbots and webchat tools to improve your users’ experience of your service.
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.
This section of the SEPs Resource Hub provides an explanation of SEP specific words and terms used throughout the guidance.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
Guidance to help you plan and prepare for implementing artificial intelligence (AI).
To help you protect, manage and enforce your intellectual property (IP) rights in Philippines.
If you’re a business, organisation or sole trader that uses PPPs and adjuvants professionally in Great Britain, register to comply with regulations.
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