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Find out the rules from 1 January 2018 if you promote or use arrangements that are meant to give someone a VAT or other indirect tax saving or a tax deferral.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Guidance on the European Union regulation on explosives precursors, including licensing, labelling and reporting suspicious activity
Form for a business to register seed marketing operations.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
The guide to VAT rules and procedures.
When and how to account for VAT when you transfer a business as a going concern (TOGC).
What you can expect us to do with your personal information when making contact with us or using our services
Find out about being 'active', trading and non-trading, and being dormant if you’re a new or existing company or organisation.
Guidance for UK companies on winning business from international aid and development projects.
The way you apply to licence biological products has changed
How veterinary medicines can be advertised.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to identify and report harmful trade practices that affect your business when exporting, importing or operating domestically.
How to renew marketing authorisations for products granted through different routes and at different times.
Guidance for the pharmaceutical industry on applying for a marketing authorisation for parallel import (MAPI).
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