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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to export or move fish for human consumption from the UK.
If you're moving goods outside the UK, you'll need to make an exit summary declaration if you've not fulfilled safety and security requirements with a full customs export declaration.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to find digital outcome, specialist and user research services on the Digital Outcomes and Specialists framework.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
Guidance on the planning for mineral extraction in plan making and the application process.
Find out the information you must give to customers on food products and how to give it.
Find a supplier who can provide user research participants to test your service with.
Guidance for suppliers and dealers.
This guidance explains the different preference tiers under the DCTS, including benefits for each tier, criteria for moving between tiers and transition periods.
How to use a quasi-experimental study to evaluate your digital health product.
Use form C&E48 to apply for authorisation to use simplified procedures for importing and exporting.
Use a Department for Education (DfE) approved framework agreement to help you buy goods and services for your school.
Join us as a Research Officer to launch a brilliant career in Government Social Research.
You're required to keep records for all traded goods you declare to HMRC for four years, for duty and tax purposes and for government statistics.
How to apply for the different simplified declarations for exports and what you need for authorisation to use them.
Subject matter specialists provide invaluable advice to Ofqual as we carry out our role in regulating qualifications. Find out how to apply to be one.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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