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Get help classifying computers, inkjet and toner cartridges and their components.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
How to use a single commodity code to import your goods in split consignments when importing large machinery or plant.
Find out what goods you do not value when when working out the VAT due on import to the UK.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out when you can use rebated diesel, biodiesel or kerosene in vehicles and other machinery.
Get help to classify footwear and parts of footwear for import and export.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Get help to classify edible vegetables, roots, tubers, herbs, spices, fruit, nuts and peel for import and export.
Apply for indefinite leave to remain ('settlement') if you have a business, investor or talent visa - fees, who's eligible, how to apply.
How to use a factorial randomised controlled trial to evaluate your digital health product.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
Organisational definitions of terms concerned with risk and risk-related matters.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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