New Speaker & Agenda Announcements

We have added two exciting new items to our upcoming 3rd Annual Executing Global Clinical Trials event 2012! 

How to Do Clinical Trials in Europe: Clarifying Confusion, Changes & Updates

1. •An update on the clinical trial approval process in Europe
2. •How to get the correct scientific advice

David R. Jones, Expert Scientific Assessor (Pharmacotoxicologist), Licensing Division, Medicines and Healthcare Products Regulatory Agency (MHRA), UK

and

Regulatory Update on Brazil/Latin America 

Renato P. Ribeiro, PhD, Clinical Research Manager - GCTO Brazil, Merck

To see the rest of the agenda, please visit here. 

For more information contact service@theconferenceforum.org.