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The civil procedure rules govern the way civil cases are managed, and set out the processes of the Civil Division of the Court of Appeal, the High Court and the County Court.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
Management of British armed forces casualties and compassionate cases 24 hours a day, 7 days a week, 365 days a year.
Interested parties can review records of applications and statements submitted to OPRED as required by environmental regulations.
The family procedure rules are a single set of rules governing the practice and procedure in family proceedings in the high court, county courts and magistrates' courts.
Information about opinions requests we have received this year
Information for companies on the import and export of controlled drugs to and from the UK.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
This project explores a new approach to command and control.
Export controls on goods that can be used for torture or capital punishment.
Find out about local procedures, burials and cremations, and returning the body to the UK.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
This page provides practical information to help you make the most of your IP when doing business in Peru.
Nigeria is subject to regional controls governing small arms and light weapons.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Information from the National Health Service on conditions, treatments, local services and healthy living
Consumer advice and details of how to report problems with e-cigarettes with guidance on how to place an e-cigarette on the market in Great Britain and Northern Ireland, including the notification scheme.
How end-use controls apply to weapons of mass destruction (WMD) related goods, software, technology and technical assistance.
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
How to use A/B testing to evaluate your digital health product.
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