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Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Volume 36 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
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.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Publish your code and use open source to improve transparency, flexibility and accountability.
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.
Volume 19 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to self-upload evidence when making an application to come to or stay in the UK.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
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