Skip to main content
Back

EVS-EN ISO 17100:2015

Translation Services - Requirements for translation services (ISO 17100:2015)

General information

Valid from 04.11.2015
Base Documents
ISO 17100:2015; EN ISO 17100:2015
Directives or regulations
None

Standard history

Status
Date
Type
Name
17.11.2017
Amendment
17.11.2017
Main + amendment
04.11.2015
Main
06.08.2007
Main
This International Standard provides requirements for the core processes, resources, and other aspects necessary for the delivery of a quality translation service that meets applicable specifications. Application of this International Standard also provides the means by which a translation service provider (TSP) can demonstrate conformity of specified translation services to this International Standard and the capability of its processes and resources to deliver a translation service that will meet the client’s and other applicable specifications. Applicable specifications can include those of the client, of the TSP itself, and of any relevant industry codes, best-practice guides, or legislation. The use of raw output from machine translation plus post-editing is outside the scope of this International Standard. This International Standard does not apply to interpreting services.

Required fields are indicated with *

*
*
*
PDF
19.52 € incl tax
Paper
19.52 € incl tax
Browse standard from 2.44 € incl tax
Standard monitoring

Customers who bought this item also bought

Amendment

EVS-EN ISO 17100:2015/A1:2017

Translation services - Requirements for translation services - Amendment 1 (ISO 17100:2015/Amd 1:2017)
Valid from 17.11.2017
Main

EVS-EN ISO 11737-1:2018

Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2018)
Valid from 15.02.2018
Main

EVS-EN 556-1:2002

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices.
Withdrawn from 15.07.2024
Amendment

EVS-EN ISO 11137-1:2015/A2:2019

Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2 (ISO 11137-1:2006/Amd 2:2018)
Newest version Valid from 02.12.2019