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An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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.
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
Form to report patients meeting the case definition.
Find details of recent trade mark applications or amendments by searching the journal
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Information about the DCIA programme, with guidance on how to participate in the Pilot competition
How to use usability testing to evaluate your digital health product.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
Find data and analysis from Census 2021 and earlier censuses.
You can make observations on the patentability of a published patent application.
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