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Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Check how much your visa application costs in the country you’re in
Apply for a Temporary Work - Creative Worker visa to work in the UK in the creative industry - eligibility, extend, bring your family.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Pharmacovigilance system requirements
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
What you need to do to work and operate in the aviation industry.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
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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