4:30
CTIS Video Tutorial - CTIS common functionalities, Part B
European Medicines Agency
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CTIS Video Tutorial - CTIS specific functionalities
European Medicines Agency
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CTIS Video Tutorial - CTIS common functionalities, Part A
European Medicines Agency
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5:20
CTIS Video Tutorial – Submitting Initial Clinical Trial Application in CTIS: Part II Section
European Medicines Agency
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4:01
CTIS Video Tutorial - How to manage the workload in CTIS - Timetable
European Medicines Agency
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1:30
CTIS Video Tutorial - How to amend and revoke roles of registered users in CTIS
European Medicines Agency
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3:00
CTIS Video Tutorial – Creating a Clinical Trial: Trial-Centric vs Organisation-Centric Approach
European Medicines Agency
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5:12
CTIS Video Tutorial – Managing a Clinical Trial in CTIS: Trial & Recruitment Notices (Sponsor)
European Medicines Agency
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4:23
CTIS Video Tutorial – Managing a Clinical Trial in CTIS Sponsor Workspace: Other Notifications
European Medicines Agency
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4:38
CTIS Video Tutorial - How to manage the workload in CTIS - RFI tab (sponsor workspace)
European Medicines Agency
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2:59:36
Clinical Trials Information System Demonstration for CTIS stakeholders – part 2- January 2022
European Medicines Agency
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6:47
CTIS Video Tutorial - How to create, cancel or clear, and submit an annual safety report
European Medicines Agency
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7:43
CTIS Video Tutorial - How to submit a substantial modification in the CTIS Sponsor workspace
European Medicines Agency
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2:06
5:12
CTIS Video Tutorial - CTIS password recovery and User profile functionalities
European Medicines Agency
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4:14
CTIS Video Tutorial – Submitting Initial Clinical Trial Application in CTIS: Trial Details
European Medicines Agency
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5:30
CTIS - M15 How to view and download CTs in the authority workspace
European Medicines Agency
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4:52
CTIS Video Tutorial – Submitting Initial Clinical Trial Application in CTIS: Form & MSC Sections
European Medicines Agency
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