ISO/IEC-GUIDE 37 Instructions for use of products by consumers

ISO/IEC-GUIDE 37 - 3RD EDITION - CURRENT
Show Complete Document History

Document Center Inc. is an authorized dealer of ISO standards.
The following bibliographic material is provided to assist you with your purchasing decision:


ISO/IEC Guide 37:2012 establishes principles and gives recommendations on the design and formulation of instructions for use of products by consumers.

ISO/IEC Guide 37:2012 is intended to be used by the following:

  • committees preparing standards for consumer products;
  • product designers, manufacturers, technical writers or other people engaged in the work of conceiving and drafting such instructions;
  • importers, regulators, inspection bodies and researchers.

The principles and detailed recommendations in ISO/IEC Guide 37:2012 are intended to be applied in combination with the specific requirements on instructions for use specified in standards for particular products or groups of products. Some model formats and wordings are suggested for inclusion in standards.

ISO/IEC Guide 37:2012 contains some practical recommendations and a proposed methodology for assessment, in order to help establish common criteria for the assessment of the quality of instructions for use.

Annexes A and B provide checklists to help principal target groups using ISO/IEC Guide 37:2012.

ORDER

Price:

$161.02        


Want this as a site license?

To find similar documents by classification:

01.120 (Standardization. General rules Including rules for the preparation of standards catalogues and management of technical documents)

03.080.30 (Services for consumers Including hotels, restaurants, washing, cleaning, removals, funerals, etc. Transport services and costs, see 03.220 Consumer information, see 97.020)

This document comes with our free Notification Service, good for the life of the document.

This document is available in either Paper or PDF format.

 

Customers who bought this document also bought:

SOR/98-282
Medical Devices Regulations (Canada)

BS-EN-ISO-14971
Medical devices. Application of risk management to medical devices

ISO-15223-1
Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements

Document Number

ISO/IEC Guide 37:2012

Revision Level

3RD EDITION

Status

Current

Publication Date

Dec. 1, 2012

Committee Number

ISO/COPOLCO