会议日程
2:00 PM — 2:30 PM
Welcome and Introduction
2:30 PM — 6:30 PM
Overview of CTIS components & functionalities, sponsor user access management, sponsors roles and permissions,
2:00 PM — 6:30 PM
Workload management - create, submit initial application, respond to Request For Information (RFI)
2:00 PM — 6:30 PM
Update an initial application - substantial & non-substantial modification, manage a clinical trial through CTIS
2:00 PM — 6:30 PM
Sponsor view, search and download options, create & submit an Annual Safety Report (ASR), Clinical Study Report (CSR) submission