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Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
Find a BFPO number, send mail to and from British forces personnel and their families
Public sector is being primed to bring innovative ideas out of government labs and onto the market with £30 million backing and new guidance.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Find out more about elections and referendums in the UK, including the general election, check who can vote in each election and how voting works.
How to use VAT margin schemes - records you need to keep, invoicing and VAT return reporting
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.
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