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Data, Freedom of Information releases and corporate reports
Apply for a Temporary Work – Government Authorised Exchange (GAE) visa for work experience, training, research or fellowship - eligibility, extend or switch, family members
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a before-and-after study to evaluate your digital health product.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 26 April 2024.
Find out how the Woodland Creation Fast Track supports quicker decisions for woodland creation proposals in low sensitivity areas.
What you need to check inside and outside of the vehicle when you do a bus, coach or other public service vehicle (PSV) walkaround check.
Using HM Land Registry’s portal, you can easily find, edit, submit and track a colleague's application.
How to use a crossover randomised controlled trial to evaluate your digital health product.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Check what customs charges apply when using a fast parcel operator to make import and export customs declarations.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
How to use a risk-based approach to carry out compulsory risk assessments of your business.
What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a case-control study to evaluate your digital health product.
Check if you can operate a facility and meet the conditions to store imported goods temporarily and find out how to apply.
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