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Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Use these forms if you import, export, or move goods through the UK.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Pharmacovigilance system requirements
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Details of expired General Licences issued by OFSI.
Find out about the requirements and obligations for warehousekeepers of motor and heating fuels in the UK.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
The Renewable Transport Fuel Obligation Order regulates renewable fuels used for transport.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
What you must do if you are a wholesaler or reseller selling fluorinated gas (F gas) in cylinders or equipment.
Look up a trade mark to see if something identical or similar to your brand is already registered.
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Nigeria is subject to regional controls governing small arms and light weapons.
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.
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