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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
Information to help you identify if your organisation needs to publish a modern slavery statement and best practice guidance on producing a statement.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to write well for your audience, including specialists.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
Management systems, policies and checks you need in place at your MOT centre to make sure MOT testing is done to the right standard.
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.
Learn how to check if your website or mobile app is accessible.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Find out about the VAT place of supply rules if your business sells digital services to private consumers.
How to identify and classify waste that contains POPs.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Reapply for a driving licence if your licence was taken away (revoked) or if you surrendered your licence following a medical condition
Guidance and advice for candidates using the Civil Service Jobs website.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
This guide provides an overview of the inspection data summary report (IDSR) for primary and secondary schools, including schools with a sixth form and gives guidance on interpreting the data.
Biosecurity and hygiene standards to keep birds safe from bird flu (avian influenza).
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