Event Date/Time: Mar 14, 2008 |
Description
WEBINAR HIGHLIGHTS
In this webinar we will look at the following documents:
•Directive 2001/20/EC (alias Clinical Trials Directive and Good Clinical Practice Directive)
•Volume 10: Notice to Applicants. Special emphasis will be given in the areas of responsibilities of the sponsor, adverse event concept, reporting rules to EudraVigilance and prerequisites for reporting to EudraVigilance.