Home » GHTF Issues Updates on Harmonizing Premarket, Postmarket and Quality Regs
GHTF Issues Updates on Harmonizing Premarket, Postmarket and Quality Regs
October 5, 2006
Three study groups of the Global Harmonization Task Force (GHTF) have issued new guidance documents dealing with harmonized approaches for conducting medical device postmarket surveillance, classification and conformity assessment and regulatory auditing of quality systems.
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