Feb 28, 2013
GPMG, a medical device consulting firm, unveiled a quality system product designed for specification developers. The FDA QSR and ISO 13485 compliant system governs all aspects of product development, design transfer, and device master records.
Feb 27, 2013
GPMG, a medical device consulting firm, unveiled a new product to help Initial Importers of medical devices comply with FDA regulations. The design of the system allows for immediate implementation and fits varying organizational structures.
Sep 25, 2012
Global Pacific Manufacturing Group llc (www.gpacmfg.com ) has developed an ISO 13485 FDA QSR compliant quality management system in a modular format designed for rapid implementation and integration.
Sep 18, 2012
Global Pacific Manufacturing Group LLC (www.gpacmfg.com ) has developed an ISO 13485 FDA QSR Compliant Quality Management System