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Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
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 about Import VAT and Customs Duty when you send gifts into the UK.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Nigeria is subject to regional controls governing small arms and light weapons.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Check the tariff classification for chewing tobacco and snuff (nasal tobacco).
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Check the tariff classification for flavour pods.
When and how to take samples for the salmonella national control programme (NCP) if you breed turkeys, and what happens if a flock tests positive.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Find out how to import timber and wood material, including the documents, identity checks and plant health inspections required.
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
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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