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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.
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.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Check the tariff classification for chewing tobacco and snuff (nasal tobacco).
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
The Multidisciplinary University Research Initiative (MURI) is a US Department of Defense (DoD) programme.
Check the tariff classification for lace-up low shoes.
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.
Reports and data on export control licensing compiled by the export control organisation.
Find data and analysis from Census 2021 and earlier censuses.
Check the tariff classification for flavour pods.
Get help to classify drones and aircraft parts for import and export.
Get help to classify organic chemicals that contain certain permitted additives or can be dissolved in water, for import and export.
Information on how UK companies can control risks when doing business in Mexico.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
This is advice for UK sponsors whose students are affected by coronavirus (COVID-19).
The CMA investigated alleged excessive and unfair pricing, anti-competitive agreements and abusive conduct with respect to hydrocortisone tablets under Chapters I and II CA98 and Articles 101 and 102 TFEU.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
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