Date :
Place : United States, New hyde park
Website :http://bit.ly/1hnvNbt
Contact Person:Roger Davis
Description:
On 16 April 2014 the new Regulation EU No 536/2014 of the European Parliament and of the Council on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC was adopted, and published in the Official Journal on 27 May 2014 (the "Clinical Trials Regulation").Deadline for abstracts/proposals : 15th September 2015
Organized By :Compliance Global Inc.
Keynote Speakers : Adriaan Fruijtier has graduated as a pharmacist at the University of Utrecht, The Netherlands. He is currently Director Regulatory Affairs at CATS Consultants. Until March 2004, he has been Head of the Oncology Group within Global Regulatory Affairs at Bayer AG, Wuppertal, Germany, and Bayer Corporation, West Haven, CT, USA. Between 2001 and 2003, he was Director of Regulatory Affairs at Micromet AG, a biotech company in Munich, Germany. Prior to joining Micromet he has worked for four years as
Conference Highlights :The webinar will start with a discussion of the disadvantages of the current situation. An overview of the Clinical Trials Regulation and the scope of the regulation will be provided. In particular the following points will be addressed: • A streamlined application procedure via a single entry point; • An EU portal and database, for all clinical trials conducted in Europe. Registration via the portal will be a prerequisite for the assessment of any application; • A single authorisatio
Venue :Online Webinar For more information, Email: [email protected] Toll Free: +1-844-746-4244 Tel: +1-516-900-5515
Check the event website for more details.