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Supplier declarations are where your UK supplier provides you with information needed to prove the origin of your goods for preferential rates of duty between the UK and other countries.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to apply for accreditation, comply with your accreditation and packaging waste technical information.
How to use a quasi-experimental study to evaluate your digital health product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Find out about the SFI actions for soils, what land is eligible for each action, and what you need to do to get paid.
How to use a factorial randomised controlled trial to evaluate your digital health product.
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Choose how you’ll make supplementary declarations for goods that you entered into your own records without authorisation.
How to charge and account for VAT on the movement of goods between Northern Ireland and EU member states (VAT Notice 725).
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.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 3 May 2024.
How to use a case-control study to evaluate your digital health product.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out how to work out your annual alcohol production if you’re part of a group, or you merge with, or separate from another business.
How to use usability testing to evaluate your digital health product.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
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