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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
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...
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Check how much your visa application costs in the country you’re in
Make sure that domains that do not send email cannot be used for spoofing.
Imposing safeguard measures for imports of certain steel products.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
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 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 China.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
Nigeria is subject to regional controls governing small arms and light weapons.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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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