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Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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 for British citizens moving to or living in Colombia, including guidance on residency, passports, healthcare and emergencies.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
How to self-upload evidence when making an application to come to or stay in the UK.
Official information for UK nationals living in or moving to Belarus, including guidance on residency, passports and healthcare.
This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
Guidance for industry on flexible approaches we are taking on good distribution practices.
You can make observations on the patentability of a published patent application.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Data on the real-world efficacy of the COVID-19 vaccines.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
Find out about tax charges on scholarships.
How end-use controls apply to weapons of mass destruction (WMD) related goods, software, technology and technical assistance.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
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