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Using metadata to make it easier to catalogue, validate, reuse and share your data.
Use this form to file a translation in connection with a European patent or a European patent application
Check how much your visa application costs in the country you’re in
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
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...
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
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
A CV is a summary of your skills, achievements and experience that you use to apply for jobs. Check advice on what to include and how to make it stand out.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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.
Volume 34 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
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 patents journal to find UK-registered patents granted, published and filed
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
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