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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
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The epidemiology, symptoms, diagnosis and management of Nipah virus infections.
Check how much your visa application costs in the country you’re in
Guidance on how to prove someone’s identity or give them access to your service or organisation.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Find out how to link your temporary storage facility to Customs Handling of Import and Export Freight (CHIEF) or the Customs Declaration Service using a Community Systems Provider.
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 Colombia.
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use supplementary pages SA109 to record your residence and domicile status on your SA100 Tax Return.
Check the tariff classification for peptide nisin standardised with sodium chloride
Check what UIDs you need for your tobacco products and the specifications they need to meet.
The requirements for packaging DNLEU
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
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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