The number of substances that are announced to be introduced in the process of REACH authorisation is considerably growing, and the authorities have 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 Annex XIV Authorisation list contains now 14 substances and the two ECHA guidance documents aimed to help companies with the preparation of an application for authorisation are available. However a lot of fields are still to be explored.
In view of the substantial acceleration of the process and the recent developments, 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 
10 July 2012
11 September 2012

Time: 15:00 to 16:30

Speaker: Vincent Navez, ReachCentrum legal expert

Price: 210 € (VAT will be applied for belgian companies only) online payment by credit card and registrations only