We need your consent to use the individual data so that you can see information about your interests, among other things. Click "OK" to give your consent.
Guide to the development and inclusion of aspects of safety in International Standards for medical devices
Translate name
STANDARD published on 12.8.2019
Designation standards: ISO/IEC/GUIDE 63:2019-ed.3.0
Publication date standards: 12.8.2019
SKU: NS-1149955
The number of pages: 26
Approximate weight : 78 g (0.17 lbs)
Country: International technical standard
Category: Technical standards ISO
Description / Abstract: This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk management concepts and methodology. This document is applicable to any aspect related to the safety of people, property, the environment, or a combination of these. In this document, the term "product" includes a medical device or a system consisting of one or more medical devices, possibly combined with non-medical devices.
Do you want to make sure you use only the valid technical standards?
We can offer you a solution which will provide you a monthly overview concerning the updating of standards which you use.
Would you like to know more? Look at this page.
Latest update: 2024-09-25 (Number of items: 2 350 354)
© Copyright 2024 NORMSERVIS s.r.o.