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How investigators and sponsors should manage clinical trials during COVID-19
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
We are here to make digital government simpler, clearer and faster for everyone. GDS is part of the Cabinet Office .
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
You must register and declare ozone-depleting substances (ODS) for laboratory or analytical uses.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guide provides information about being arrested in Germany and what conditions are like in prison there.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
How to self-upload evidence when making an application to come to or stay in the UK.
The requirements for packaging HHGW
How to get fast-track approval of medical devices during COVID-19.
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