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A guide to collecting data about your packaging. This is for UK organisations affected by extended producer responsibility (EPR) for packaging.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
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.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Following MHRA approval of a clinical trial, early breast cancer patients on endocrine-based therapy can benefit from a study with camizestrant.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
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