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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
A guide on what to look out for when signing up to a cloud storage service.
Transitional methods of measurement in relation to ecodesign for use prior to the designation of relevant standards.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Guidelines for civil panel counsel, revised to include the new government security classifications.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to manage a temporary storage facility, how to handle goods, what records to keep, how to increase the size of, or move goods between facilities.
Environment Agency regulatory position on when you can store and shred electronic storage media containing confidential or sensitive material for data security and destruction only without an environmental permit.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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