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Volume 51 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Volume 36 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
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...
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Look up a trade mark to see if something identical or similar to your brand is already registered.
Apply for a Global Talent visa to work in the arts, sciences or digital technology once you have been endorsed as a leader or potential leader.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
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.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Form to report patients meeting the case definition.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
You can make observations on the patentability of a published patent application.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Volume 52 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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