www.fdanews.com/articles/123231-ghtf-advises-devicemakers-on-nonconforming-products
GHTF Advises Devicemakers on Nonconforming Products
December 28, 2009
Devicemakers may need to validate, as well as verify, preventive actions taken to avoid the recurrence of nonconformities, according to a new guideline proposed by the Global Harmonization Task Force (GHTF). The guideline, issued by Study Group 3 and recently posted to the GHTF website, advises manufacturers on
measurement, analysis and improvement for corrective and preventive actions. Comments are due April 25.
International Medical Device Regulatory Monitor
International Medical Device Regulatory Monitor