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How to comply with the regulatory requirements for manufacturing custom-made medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
When you do and do not have to offer a refund, repair or replacement, unconditional refunds for online purchases, and penalties for deceiving customers
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to conform with the legal requirements for placing medical devices on the market.
Get help to classify textiles and which headings and codes to use.
Case study from Holistic AI.
Self-build and custom housebuilding registers.
This review found no sources of straightforward indicators for use in measuring diplomatic influence
Improving how people qualify to become an approved driving instructor (ADI) and other changes to the ADI register.
An alternative to conventional methods for cloning hard-to-clone gene segments in the influenza reverse genetics system.
Exploring the educational barriers facing adolescents in Cox’s Bazar
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