Medical device software. Software life-cycle processesWhat is this standard about? It deals with medical device software. The amendment adds requirements for legacy software which will help manufacturers demonstrate compliance with the relevant European Directives. Who is this standard for? The standard is relevant to manufacturers of: Medical electrical equipment Medical devices incorporating software Software that is itself a medical device Why should you use this standard? The amended standard applies

BS EN 50395 provides best industry guidance on the Insulation resistance test

In addition to making recommendations intended to establish the basic requirements for life safety

Reference list of the tables of mechanical properties of the relevant aluminium and aluminium alloys

BS EN 13431 guidelines help you in packaging recoverable for energy recovery and ensure that hazardous constituents of packaging should have a minimal impact on the environment

PAS 221 is part of a series of PASs which tackle different elements of the food chain

These systems

the general technical delivery requirements of BS EN 10021 are applicable

BS EN 61511-2 provides guidance on the specification

This standard is applicable to axles that are designed in accordance with the requirements of EN 13103 and EN 13104

It should also be of particular interest to anyone who has bought BS EN ISO 14001

Characteristics of pans for testing on electric cooking plates

processed or used