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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.
The technical writing community is for anyone who wants to discuss and learn about the role of technical writing in government.
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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
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Explains how to make sure people can find your data and how to maintain it.
A series of blog from Parole Board CEO Martin Jones on the work of the Parole Board
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How to use a cost benefit analysis to evaluate your digital health product.
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