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Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a cost benefit analysis to evaluate your digital health product.
Find out what goods you do not value when when working out the VAT due on import to the UK.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
VAT and other taxes on shopping and services, including tax-free shopping, energy-saving equipment and mobility aids.
Use this form to appeal to the First-tier Tribunal (Environment) against a decision to include your land, or part of it, in a nitrate vulnerable zone.
How to use a quasi-experimental study to evaluate your digital health product.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Get help to classify electrical equipment such as communication equipment, cameras, and their parts and accessories.
Examples of viral haemorrhagic fevers (VHFs) include Lassa fever, Crimean-Congo haemorrhagic fever, Marburg and Ebola virus diseases.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Find helpsheets, forms and notes to help you fill in the capital gains pages of your Self Assessment tax return.
Information and guidance for local authorities compiling the P1E quarterly data returns on homelessness.
Find out what areas the Scottish administration legislates on and how it is structured.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to apply for marketing authorisation via this new procedure.
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