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GPMG Product Helps Medical Device Specification Developers be FDA and ISO 13485 Compliant
Date:2/28/2013

  • Align each procedure with the manufacturer's organization structure, activity, and preferences 
  • Train core staff in a logical sequence
  • Provide ongoing support until certification.
  • GPMG is confident medical device specification developers seeking ISO 13485 certification and FDA QSR compliance will take full advantage of this cost-effective solution.

    About GPMG:

    Global Pacific Manufacturing Group LLC is a privately held medical device consulting firm that assists medical device manufacturers with product development and regulatory compliance globally.

    To learn more about Global Pacific Manufacturing Group LLC products and services visit them at:  www.gpacmfg.com

    Media Contact Information:

    Aaron Lyon
    Global Pacific Manufacturing Group
    202-380-9380 (office)

    PRLog ID: www.prlog.org/12087572


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    SOURCE Global Pacific Manufacturing Group LLC
    Copyright©2012 PR Newswire.
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