Publikuar
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.
                    PUBLISHED
                    DS ISO/IEC Udhëzues 63:2019
                    60.60
                                        Standard published
                    20 jan 2021