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Role of Standards in the Assessment of Medical Devices Study Group 1 Final Document GHTF/SG1/N044:2008
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Document Date: 2012-11-13 17:52:34


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File Size: 94,00 KB

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Authoring Group / /

IndustryTerm

internal manufacturer / to all products / similar products / risk management / distribution chain / regulatory systems / particular device / sterile medical devices / individual manufacturer / voluntary / supply medical devices / diagnostic medical devices / /

Organization

Task Force / Regulatory Authority / Global Harmonization Task Force / /

Position

Chair / global regulatory model for medical devices / /

PublishedMedium

Conformity / /

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