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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.
Use the online service or postal form C1454 if you're an exporter and want to use Simplified Procedures to export preference qualifying goods to preference-giving countries.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
You can renew a registered design or restore a design that's expired with the Intellectual Property Office
The cases we most commonly handle are disputes relating to: personal injury negligence breach of contract breach of a statutory duty breach of the Human Rights Act 1998 libel, slander and other torts non-payment of a debt and ‘enforcement orders’...
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Find the difficulty level of a qualification and compare qualifications across different countries.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
Events courses and programmes to develop skills, knowledge and networks for chief executive officers, deputy-CEOs and their equivalents in public service.
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
The government introduced a number of measures through the Levelling Up and Regeneration Act 2023 to incentivise the prompt build-out of housing sites. This update outlines recent progress in the implementation of these measures and next steps.
Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Use this online service to complete a form or send additional documents for a UK patent you've already applied for (a patent pending)
Working with contract management and accreditation.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
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