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Use this form to file a translation in connection with a European patent or a European patent application
Pharmacovigilance system requirements
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...
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
The family procedure rules are a single set of rules governing the practice and procedure in family proceedings in the high court, county courts and magistrates' courts.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Check how much your visa application costs in the country you’re in
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Understand how to use artificial intelligence ethically and safely
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance for those producing, processing, consuming, importing or exporting chemicals covered by the Chemical Weapons Convention (CWC)
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
QCA was responsible for maintaining and developing the national curriculum and associated assessments, tests and examinations; and accredited and monitored qualifications in colleges and at work.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
A suite of template legal documents to support the development of mutuals.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
How to self-upload evidence when making an application to come to or stay in the UK.
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