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How to use a micro-randomised trial to evaluate your digital health product.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Assessment framework specification files for software suppliers developing management information systems (MIS).
A trust is a way of managing assets (money, investments, land or buildings) for people - types of trust, how they are taxed, where to get help.
Outlines changes in methodology and reporting in building materials statistics.
A capitated approach to payment for mental health services with outcomes and risk share.
Making legacy and future air mission systems affordable, capable and adaptable by adopting an open systems architecture approach and systematic software re-use.
Get help classifying computers, inkjet and toner cartridges and their components.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
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