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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.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
How to self-upload evidence when making an application to come to or stay in the UK.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
Information on embargoes on West African States and how to apply for an export licence.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Check the tariff classification for flavour pods.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Export controls on goods that can be used for torture or capital punishment.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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