Global Pacific Manufacturing Group LLC

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.

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.

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.

Global Pacific Manufacturing Group LLC (www.gpacmfg.com ) has developed an ISO 13485 FDA QSR Compliant Quality Management System