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Check what you need to do to employ teachers who are non-UK citizens.
Check how much your visa application costs in the country you’re in
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
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
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
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