QUESTIONS| Event Date/Time: Mar 14, 2008 |
Report as SpamDescription
Join us online for a 90 minute webinar to learn more about SUSAR Reporting for Interventional Clinical Trials in the EEA.
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.
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.
