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How to use feedback from marketplace reviews to evaluate your digital health product.
Guide for overseas investors on how to access NHS procurement channels.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
The Committee on Mutagenicity of Chemicals in Food, Consumer Products and the Environment (COM) assesses and advises on mutagenic risks to humans. COM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care and the...
The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
You can reserve books and other items such as DVDs at your local library - contact your council for more information
How to charge and account for VAT on the movement of goods between Northern Ireland and EU member states (VAT Notice 725).
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Report treasure finds to the local coroner within 14 days - items officially defined as treasure, Portable Antiquities Scheme, inquest, valuation, rewards
Claim relief on import duty and VAT when importing miscellaneous documents and related articles into the UK.
Guidance for UK companies on winning business from international aid and development projects.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out about which goods and services for disabled people and people aged 60 or over that you should apply zero or reduced rate VAT.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
The Reviewing Committee on the Export of Works of Art and Objects of Cultural Interest (RCEWA) advises the government on the export of cultural property. If an artwork is sold to a foreign buyer, it also advises on whether to...
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
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