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Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Use this form to file a translation in connection with a European patent or a European patent application
Make sure that domains that do not send email cannot be used for spoofing.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
What you need to do to work and operate in the aviation industry.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Find out which radioactive sources you need a licence to export and how to apply for one.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Check the tariff classification for flavour pods.
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.
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
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