The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices, Second Edition PDF

The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices, Second Edition PDF

Name:
The FDA and Worldwide Quality System Requirements Guidebook for Medical Devices, Second Edition PDF

Published Date:
06/06/2008

Status:
Active

Description:

Publisher:
American Society for Quality

Document status:
Active

Format:
Electronic (PDF)

Delivery time:
10 minutes

Delivery time (for Russian version):
200 business days

SKU:

Choose Document Language:
Need Help?
This new and expanded second edition maintains the organizational approach of the first and includes the requirements and guidance contained in the Quality System Regulation (QSReg), the ISO 13485:2003 standard, the ISO/TR 14969:2004 guidance document, and, as appropriate, a number of the FDA and Global Harmonization Task Force (GHTF) guidance documents.

This second edition also addresses a number of additional topics, such as the incorporation of risk management into the medical device organization's QMS, QMS issues related to combination products, the key process interactions within a QMS, effective presentation of and advocacy for a QMS during FDA inspections and third-party assessments, and future FDA compliance and standards activities.

The organization of the guidebook is based on the order of the requirements in the QSReg. For each substantive requirement section there is:
  • A verbatim statement of the QSReg requirement.
  • A description of the comparable requirement in ISO 13485:2003, focusing on any additions to or differences from the requirements contained in the QSReg.
  • Excerpts of the FDA responses to relevant comment groups contained in the Preamble to the QSReg.
  • Excerpts from various FDA guidance documents related to quality management systems.
  • A description of the relevant guidance contained in ISO/TR 14969:2004, focusing on any additions to or differences from the guidance in the Preamble and other FDA guidance documents, and, if useful, excerpts from relevant GHTF guidances.
  • Authors' notes giving guidance derived from the authors' sixty years of regulatory compliance experience.


This guidance book is meant as a resource to manufacturers of medical devices, providing up-to-date information concerning required and recommended quality system practices. It should be used as a companion to the regulations/standards themselves and texts on the specific processes and activities contained within the QMS.
Edition : 2nd
ISBN(s) : 9780873897402
Number of Pages : 336
Published : 06/06/2008

History


Related products

ASQ S2-1995
Published Date: 01/01/1995
Introduction to Attribute Sampling
$17.7

Best-Selling Products

AVIXA A102.01
Published Date: 04/11/2017
Audio Coverage Uniformity in Listener Areas
$22.5
AVIXA ANSI/INFOCOMM 10
Published Date: 12/20/2013
Audiovisual Systems Performance Verification
$22.5
AVIXA ANSI/INFOCOMM 2M
Published Date: 12/05/2010
Standard Guide for Audiovisual Systems Design and Coordination Processes
$22.5
AVIXA ANSI/INFOCOMM 3M
Published Date: 06/30/2011
Projected Image System Contrast Ratio
$22.5
AVIXA ANSI/INFOCOMM 4
Published Date: 06/19/2012
Audiovisual Systems Energy Management
$22.5
AVIXA F501.01
Published Date: 12/31/2015
Cable Labeling for Audiovisual Systems
$22.5