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Exporters of groups of products of animal origin (POAO) to the EU and Northern Ireland can join the groupage export facilitation scheme (GEFS) to use 30-day support attestations.
How to prepare and analyse the data you collected for your evaluation.
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 write up and share your findings
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
Sets out the process for pharmaceutical companies to appeal against decisions made by the Secretary of State for Health and Social Care.
Check the tariff classification for vitamin gummies.
How to use a budget impact analysis to evaluate your digital health product.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
An update regarding the European Commission's Working Group meeting on nutrition and health claims,17 September 2012, was issued to interested parties on the 25 September 2012.
How to use a cost effectiveness analysis to evaluate your digital health product.
We want your views on changes being proposed to Advisory Committee on Borderline Substances (ACBS) policy about standard adult ready-to-drink oral nutritional supplements listed in part XV of the Drug Tariff.
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