Obelis is pleased to announce that EG MONT, Obelis’ Official Representative in Brazil, in association with HI-POWER, MEDLAB, and CENIC will be conducting a workshop in Sao Paulo, Brazil concerning the application and revisions of the CE marking as pertaining to the current European Union Directives. This workshop will focus on the CE marking as it applies to Medical Devices, In-Vitro Diagnostic Devices and how the Waste Electrical and Electronic Equipment (WEEE) and the Restriction of Hazardous Substances (RoHS) Directives influence such devices to be placed onto the European Market.
The WEEE Directive promotes the recycling of Electrical and Electronic Equipment and their components at end-of-life or when being replaced. The RoHS Directive specifies maximum levels for restricted hazardous substances in the manufacture of various types of Electrical and Electronic Equipment.
The process of CE Certification is increasingly important as the CE marking is continually becoming a global marking of safety and quality for regulatory principles around the world.
As medical and diagnostic devices become increasingly more complex concerning the electrical components and substances which they use, understanding how the WEEE and RoHS Directives influence your products is vital to success in the European Market and abroad.
The Workshop will be held on the follow dates and locations:
Time: 08h00-16h00
Date: 29th and 30th of June, 2011.
Location: Av. Paulista, 1776-2o Andar – Auditorio Umuarama (estacao Trianon – MASP do metro)
Those who register for the event may receive individual meetings with the Workshop presenters who are experts and business professionals with many years of experience in the topics that will be presented.