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DIN EN 60812

Failure Mode and Effects analysis (FMEA) (IEC 56/1579/CD:2014)

pending
Organization: DIN
Publication Date: 1 August 2015
Status: pending
Page Count: 144
ICS Code (Characteristics and design of machines, apparatus, equipment): 21.020
ICS Code (Quality in general): 03.120.01
ICS Code (Electrical engineering in general): 29.020

Document History

DIN EN 60812
August 1, 2015
Failure Mode and Effects analysis (FMEA) (IEC 56/1579/CD:2014)
A description is not available for this item.
DIN EN 60812
November 1, 2006
Analysetechniken fuer die Funktionsfaehigkeit von Systemen - Verfahren fuer die Fehlzustandsart- und -auswirkungsanalyse (FMEA) (IEC 60812:2006); Deutsche Fassung EN 60812:2006
A description is not available for this item.

References

This document is referenced by:
VDI 4007 - Reliability goals - Determination, check, review, certificate
Published by VDI on June 1, 2012
This VDI Guideline is applicable regardless of the industry. It is a supplement and in-depth treatment of the guideline VDI 4003, which describes a general framework for organising, steering and...
This document is referenced by:
VDI 4003 - Reliability management
Published by VDI on March 1, 2007
Scope of application This guideline serves as an aid in planning, steering, implementation and control of reliability work in an organization. Responsibility for reliability management and the...
This document is referenced by:
DIN EN ISO 13408-1 - Aseptische Herstellung von Produkten fuer die Gesundheitsfuersorge - Teil 1: Allgemeine Anforderungen (ISO 13408-1:2008, einschliesslich Amd 1:2013); Deutsche Fassung EN ISO 13408-1:2015
Published by DIN on December 1, 2015
Der vorliegende Teil von ISO 13408 legt die allgemeinen Anforderungen an Verfahren, Programme und Verfahrensweisen zur Entwicklung, Validierung und Routinekontrolle des Herstellungsverfahrens für...
This document is referenced by:
DIN EN ISO 13408-1 - Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)
Published by DIN on December 1, 2015
This part of ISO 13408 specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing...
This document is referenced by:
DIN EN ISO 15378 - Primaerpackmittel fuer Arzneimittel - Besondere Anforderungen fuer die Anwendung von ISO 9001:2015 entsprechend der Guten Herstellungspraxis (GMP) (ISO 15378:2017); Deutsche Fassung EN ISO 15378:2017
Published by DIN on April 1, 2018
Diese Internationale Norm legt Anforderungen an ein Qualitätsmanagementsystem fest, wenn eine Organisation a) ihre Fähigkeit darlegen muss, beständig Produkte und Dienstleistungen bereitstellen zu...
This document is referenced by:
DIN EN ISO 15378 - Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017)
Published by DIN on April 1, 2018
This International Standard specifies requirements for a quality management system when an organization: a) needs to demonstrate its ability to consistently provide products and services that meet...
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