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Find information on completing the partnership section of your Self Assessment tax return.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Find out what information you need to send HMRC before you make a claim for R&D Corporation Tax relief.
The review of the safety of isotretinoin has concluded.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
FCDO travel advice for USA. Includes safety and security, insurance, entry requirements and legal differences.
This guidance relates to Technical Standards and Standard Development Organisations to describe the typical first step in a Standard Essential Patent (SEP) journey.
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