A Practical Field Guide for ISO 13485:2016 Medical Devices--Quality Management Systems--Requirements for Regulatory Purposes
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Sprache:Englisch
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57,49 €
inkl. MwStBeschreibung
Details
Format
ePUB
Kopierschutz
Ja
Family Sharing
Nein
Text-to-Speech
Ja
Erscheinungsdatum
06.11.2019
Verlag
ASQ Quality PressSeitenzahl
153 (Printausgabe)
Dateigröße
7136 KB
Auflage
1. Auflage
Sprache
Englisch
EAN
9781951058210
The purpose of this expanded field guide is to assist organizations, step-by-step, in implementing a quality management system (QMS) in conformance with ISO 13485:2016, whether "from scratch" or by transitioning from variations of the ISO 13485 family. In keeping with ISO 9000:2015's definition of quality as the "degree to which a set of inherent characteristics fulfills requirements," Myhrberg, Raciti, and Myhrberg have identified the requirements and inherent characteristics (distinguishing features) for this expanded field guide. Within the guide, each subclause containing requirements is the focus of a two-page visual spread that consistently presents features that fulfill the requirements listed below.
This guide will:
Provide a user-friendly guide to ISO 13485:2016's requirements for implementation purposes
-Identify the documents/documentation required, along with recommendations on what to consider retaining/adding to a QMS during ISO 13485:2016 implementation
-Guide internal auditor(s) regarding what to ask to verify that a conforming and effective QMS exists
-Direct management on what it must do and should consider to satisfy ISO 13485:2016's enhanced requirements, as well as on the responsibilities for top management
-Depict step-by-step in flowchart form what must occur to create an effective, conforming QMS
This guide will:
Provide a user-friendly guide to ISO 13485:2016's requirements for implementation purposes
-Identify the documents/documentation required, along with recommendations on what to consider retaining/adding to a QMS during ISO 13485:2016 implementation
-Guide internal auditor(s) regarding what to ask to verify that a conforming and effective QMS exists
-Direct management on what it must do and should consider to satisfy ISO 13485:2016's enhanced requirements, as well as on the responsibilities for top management
-Depict step-by-step in flowchart form what must occur to create an effective, conforming QMS
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