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Data, Freedom of Information releases and corporate reports
Find out how to account for VAT schemes on business gifts, samples and promotional schemes.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find out which stocks and shares you can purchase, make or hold in an investor's stocks and shares ISA.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
We advance prosperity by ensuring no viable UK export fails for lack of finance or insurance, doing that sustainably and at no net cost to the taxpayer.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Guide for overseas investors on how to access NHS procurement channels.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
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.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How to apply to provide digital technologies under the Help to Grow: Digital scheme if you're a software vendor.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
What you need to do if you sell or store tobacco products in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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