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Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to report incidents, including pro-formas for PON1 and PON2 and guidance on completion; listing of environmental alerts for operators in the North Sea.
First published during the 2022 to 2024 Sunak Conservative government
Phase 2 report
Information on the types of report, including pre-sentence reports, how they are used and what they should contain. It also includes information on how to manage court orders and specific requirements including electronic monitoring, unpaid work and intensive supervision and...
This rapid desk-based study was commissioned by the Department for International Development
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