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Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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
Find out how to do a rapid lateral flow test for COVID-19. Rapid lateral flow tests show the result on a device that comes with the test.
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.
Find out when and how to take samples for testing, and what happens if one of your flocks tests positive.
Find out how the ATA Carnet works, what to do at customs, and what happens if your goods are lost, destroyed or stolen.
How to self-upload evidence when making an application to come to or stay in the UK.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Rules for feeding, watering, prioritising, holding animals for slaughter, and the design and layout of a slaughterhouse.
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 on how to prove someone’s identity or give them access to your service or organisation.
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.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
Check the tariff classification for flavour pods.
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