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Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Helping public health practitioners conducting evaluations on how to plan them.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Publish your code and use open source to improve transparency, flexibility and accountability.
The Board was responsible for safeguarding and advancing public health by assuring the quality and safety of biologicals, through its management of the National Institute for Biological Standards and Control (NIBSC). In July 2008 the Health and Social Care Act...
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
What you need to do to work and operate in the aviation industry.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Find out how to import timber and wood material, including the documents, identity checks and plant health inspections required.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
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
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
The MHRA is part of the Access Consortium along with the Therapeutic Goods Administration, Health Canada, Health Sciences Authority of Singapore and Swissmedic.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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