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Media type:
E-Book
Title:
Enhancing the effectiveness of medical device incident reporting
:
final report of the EU pilot on the manufacturer incident reporting form (MIR form)
Footnote:
Bibl
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Description:
Use of globally harmonised nomenclature for adverse event reporting of medical devices is a key prerequisite for effective safety monitoring of devices in the interest of patient protection. This report analyses the results of an EU pilot project on nomenclature use and makes recommendations.