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This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How someone in Poland can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Get information on teacher training courses, funding, pay scales and how to make a great application
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...
Apply for a UK Ancestry visa if you're a Commonwealth citizen and can prove that one of your grandparents was born in the UK - eligibility, fees, documents, how to apply, how long it takes and how to settle
Pharmacovigilance system requirements
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check how much your visa application costs in the country you’re in
Make sure that domains that do not send email cannot be used for spoofing.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
We are here to make digital government simpler, clearer and faster for everyone. GDS is part of the Cabinet Office .
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.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
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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