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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
Businesses can form a partnership with a local authority to provide advice other local regulators must respect.
Guidance on using non-investigational medicinal products in a clinical trial.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
Guidance on labelling for medicinal products used in clinical trials.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Find out how to claim a customs duty waiver if you are bringing goods into Northern Ireland from Great Britain or countries outside the UK and EU which might otherwise be charged ‘at risk’ tariffs.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
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