アジェンダ
9:00 AM — 9:30 AM
Welcome and Introduction
9:30 AM — 1:30 PM
Overview of CTIS components & functionalities, sponsor user access management, sponsors roles and permissions,
9:00 AM — 1:30 PM
Create, submit, cancel and withdraw an initial application, respond to Request For Information (RFI)
9:00 AM — 1:30 PM
Update an initial application - substantial & non-substantial modification, manage a clinical trial through CTIS
9:00 AM — 1:30 PM
Sponsor view, search and download options, create & submit an Annual Safety Report (ASR), Clinical Study Report (CSR) submission