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:
鈥irective 2001/20/EC (alias Clinical Trials Directive and Good Clinical Practice Directive)
鈥olume 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:
鈥irective 2001/20/EC (alias Clinical Trials Directive and Good Clinical Practice Directive)
鈥olume 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.
