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Get information on teacher training courses, funding, pay scales and how to make a great application
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Pharmacovigilance system requirements
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
Understand how to use artificial intelligence ethically and safely
How to contact MHRA for specific services or enquiries.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Make sure that domains that do not send email cannot be used for spoofing.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Guidance on how to report a security vulnerability on any Ministry of Defence service or system, such as the websites of the Royal Air Force, British Army and Royal Navy.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Information and advice on rabies, the viral infection of the central nervous system which affects mammals and humans.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Information on the role of the Defence Industry WARP and how to report security incidents from within industry.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
Nigeria is subject to regional controls governing small arms and light weapons.
Decision on application for authorisation under UK REACH.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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