All medical equipment placed on the market in Europe must meet the requirements of either the Medical Devices Directive or the In Vitro Diagnostic Medical Devices Directive. Due to the importance placed on issues of safety within the medical world the requirements of the applicable Directive must be strictly applied by manufacturers wishing to place their products on the market in Europe.
Technology International provides technical advice and support to clients whose products need to meet either of the Medical Devices Directives. Our services include offering general advice on the scope and workings of the Directives, reviewing product designs against the requirements of both Directives and assistance with the preparation of compliance documentation.
Our goal is to help clients find the most relevant and cost-effective methods to demonstrating compliance to the Medical Devices Directives.
For more information on the Medical Devices Sector, please see the relevant section of the Europa Website.
Copyright © 2007 - 2012 Technology International (Europe) Ltd