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Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Learn how the Government Digital Service is monitoring accessibility under the Public Sector Bodies (Websites and Mobile Applications) (No.2) Accessibility Regulations 2018.
Find out how to use tools like Google Analytics and Content Data to get data on how users are interacting with GOV.UK content and improve search engine optimisation (SEO).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance and good practice for publishers on GOV.UK, including how to use publishing applications, when content belongs on GOV.UK and how to request support.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
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