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Pharmacovigilance system requirements
Look up a trade mark to see if something identical or similar to your brand is already registered.
Find out about changes to the deemed domicile rules for Income Tax and Capital Gains Tax from 6 April 2017.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out what VAT checks you must carry out on overseas sellers if you're an online marketplace operator, and what HMRC will do if you do not meet their requirements.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
Check the tariff classification for flavour pods.
Application form ID3 to prove your identity when lodging an application to HM Land Registry.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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