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Check the regulations on aircraft parts imported with a certificate of airworthiness.
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...
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Licensing requirements for importers and exporters, duty rates, reliefs and import VAT for printed books, newspapers and related products.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Use this form to file a translation in connection with a European patent or a European patent application
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
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
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
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.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Check how much your visa application costs in the country you’re in
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
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