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Blogs where government organisations talk about their work and share information and ideas.
How and when to publish a blog.
The Government Digital Service (GDS) blog about how the government is transforming digital public services.
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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
News and updates for commercial vehicle operators and drivers from the Driver and Vehicle Standards Agency (DVSA).
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Find details here about the GOV.UK blogging platform privacy policy and how we collect and process your data.
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
Advice and information for MOT garages and testers.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How investigators and sponsors should manage clinical trials during COVID-19
The International Tech Hub Network (ITHN) works to forge innovation partnerships between the UK and international tech sectors, stimulate local digital economies, and build high-end digital skills to drive sustainable jobs and growth.
Explains how to make sure people can find your data and how to maintain it.
Provides further information in support of the implementation of waste planning policy.
The home page for DSIT’s work supporting the secure and sustainable deployment of connected places technology, also known as smart cities.
How to use a cost benefit analysis to evaluate your digital health product.
Information about the eight-toothed spruce bark beetle, including how to report sightings.
Advice on how to stay secure online from the UK's National Cyber Security Centre.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
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