Global Pacific Manufacturing Group LLC

     "
Your Source for Medical Device Consulting Services"




<meta name="norton-safeweb-site-verification" content="ryjamed3es6e85jgxi483wa0txdrdz-mu3pyxocq5p-bq8p-g7g7hcehbgjhc6-o5vv3pkcih8mqrsipqwfzvu9jmexrb-k0gyzfj2whu7w9z7be8s1ayb2j8dey8tvy" />

Supplier Management

                                                SUPPLIER MANAGEMENT PROCEDURE

Supplier Management ProcedureThe supplier management procedure establishes processes to ensure that suppliers of purchased product and services intended for use in the design and manufacture of finished medical devices conform to specified requirements. Evaluation of the company’s suppliers of components, services or finished goods, the grandfathering of suppliers, and the frequency and content of supplier evaluations are addressed with this procedure.

The procedure includes step by step instruction for approving a supplier, reviews of supplier performance and condition, how to respond to deficiencies or non-conformances is supplier systems, and forms to be used throughout the approval process.

Referenced Documents:
LIST 0004  Approved Supplier List
QMSM   Quality Management System Manual
F
ORM 0011  Supplier Evaluation and Approval Form
FORM  0012  Supplier Self-Assessment Form

List of Additional GPMG Procedures

Contact us:
Office: 202-380-9380
Fax: 815-550-1702
email: info@gpacmfg.com
  

Global Pacific Manufacturing Group
120 Old Colonial Drive, Suite 4 Gardner, MA 01440 US
Phone: 202-380-9380 Website: www.gpacmfg.com

FDA 510k medical device submissions, medical device process validation, medical device sterile packaging validations, medical device ISO 13485 quality system, medical device FDA QSR compliant quality systems, FDA QSIT audit preparation, FDA consulting, accelerated aging protocols, FDA QSR audits, ISO 13485 quality system certification support, modular iso 13485 quality system product, ISO 13485 quality system procedures