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How to use a quasi-experimental 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.
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Resources to help anyone developing or running a digital health product to conduct an evaluation.
If you’re a business, organisation or sole trader that uses PPPs and adjuvants professionally in Great Britain, register to comply with regulations.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
Use these general provisions to help you determine the origin of your products.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Get a preferential rate on goods you import to the UK from a Developing Countries Trading Scheme country.
How to use a cost benefit analysis to evaluate your digital health product.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
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.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Competent authorities of exporting countries should use the relevant model health certificate as a template to create a version exporters can apply for to export other animal by-products to Great Britain, the Channel Islands or Isle of Man.
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