internal manufacturer / to all products / similar products / i.e. devices / particular device / regulatory systems / sterile medical devices / medical devices / individual manufacturer / voluntary / marketed device / /
Organization
Central office of the IEC / International Organisation for Standardization Address / Task Force / European Union / Regulatory Authority / Global Harmonization Task Force / / /
Position
global regulatory model for medical devices / Chairman / Secretary / /
Role of Standards in the Assessment of Medical Devices Study Group 1 Proposed Document SG1(PD)/N044