The number of substances that are announced to be introduced in the process of REACH authorisation is considerably growing, and the authorities have recently confirmed that the implementation of the authorisation process is now a top priority.

Expectations are high from the different stakeholders, the legislation is very detailed and many formal steps have to be followed. At the same time, the first Annex XIV Authorisation list of six substances has been published and ECHA has recently released two guidance documents aimed to help companies with the preparation of a application for authorisation. However a lot of fields are still to be explored.
In view of a substantial acceleration of the process in the coming months, this is the right time to prepare you for this other  important part of REACH. 

Get to know the new Authorisation phase

This webinar will cover a number of areas that should help you to get familiar with the main aspects of the authorisation.

Our ReachCentrum legal advisor will present these topics and will endeavour to respond to the questions raised during the webinar.

Content
-the purpose, the scope and general principles of the Authorisation 
-the different phases (timelines, etc)
-the different actors involved in the process (ECHA, the ECHA Committees, the Commission, etc)
-the way companies may organise their application
-the comparison and interface between authorisation and restriction

Target audience
Company lawyers, regulatory REACH managers, REACH project managers.

Date 
3 May 2012

Time: 15:00 to 16:30

Speaker: Vincent Navez, ReachCentrum legal expert

Price: 210 € (exclusive VAT) online payment by credit card and registrations only