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Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
How to self-upload evidence when making an application to come to or stay in the UK.
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
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Find out when and how to take samples for testing, and what happens if one of your flocks tests positive.
How to use A/B testing to evaluate your digital health product.
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.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
Share your reference data for use in projects and services outside your organisation.
Find data and analysis from Census 2021 and earlier censuses.
Understand how to manage a project which uses artificial intelligence.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
Examples of unacceptable trade marks around protected emblems, internet domain names and your company name.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
Find details of recent trade mark applications or amendments by searching the journal
Form A64A: Application to receive information from court records about a parental order.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Template China Strategic Prosperity Fund programme activity based budget.
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