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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.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The BBC (British Broadcasting Corporation) is a British public service broadcaster. Its main responsibility is to provide impartial public service broadcasting in the UK, Channel Islands and Isle of Man. BBC is a public corporation of the Department for Culture,...
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
VisitBritain (VB) is the national tourism agency, responsible for marketing Britain worldwide and developing Britain’s visitor economy. It works with UK Trade & Investment as well as airlines, travel operators, global brands and the official tourism bodies for London, England,...
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...
Make sure that domains that do not send email cannot be used for spoofing.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Report allegations of malpractice to Ofqual and understand what to expect from us
Information and advice on rabies, the viral infection of the central nervous system which affects mammals and humans.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
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