Tutorial, "Regulatory aspects of clinical trials, from IND to submission”

Thursday, 15th May 2014 at 7pm - 9pm

Location: Maison des Associations, room Rene Dumont

Clinical Trials are an essential part of any drug development. This tutorial will  provide an overview of the regulatory framework to obtain Clinical Trial approval in Europe and USA and discuss the challenges for First in Man and multinational trials.

The presenter, Dr. Brigitte Happ (Happ-Consulting), is an expert regulatory professional with  20 years of global drug development experience in Pharma/Biotech.

There will be a charge of 10 CHF for this event.



Read more http://groupspaces.com/GenevaPharmaNetwork/item/641224