Media Summary: Training module: How to create and submit an Annual Safety Report and respond to related Requests for Information. This Training module: Create, submit and withdraw a clinical trial application (Sponsors). The Training module: How to respond to RFIs received during the evaluation of a Clinical Trial Application. This

Ctis Video Tutorial Managing A - Detailed Analysis & Overview

Training module: How to create and submit an Annual Safety Report and respond to related Requests for Information. This Training module: Create, submit and withdraw a clinical trial application (Sponsors). The Training module: How to respond to RFIs received during the evaluation of a Clinical Trial Application. This Notifications and supervision activities 00:00

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CTIS Video Tutorial – Managing a Clinical Trial in CTIS: Trial & Recruitment Notices (Sponsor)
CTIS Video Tutorial – Creating a Clinical Trial: Trial-Centric vs Organisation-Centric Approach
CTIS Video Tutorial – Managing a Clinical Trial in CTIS Sponsor Workspace: Other Notifications
CTIS Video Tutorial - How to manage the workload in CTIS - Timetable
CTIS Video Tutorial - How to manage the workload in CTIS - RFI tab (sponsor workspace)
CTIS Video Tutorial - How to create, cancel or clear, and submit an annual safety report
CTIS Video Tutorial - How to submit a substantial modification in the CTIS Sponsor workspace
CTIS Video Tutorial - How to respond to RFI considerations and submit an RFI response
CTIS Video Tutorial - CTIS specific functionalities
CTIS Bitesize talk
Preparing Content for CTIS & the EU CTR
CTIS Video Tutorial - How to request roles and how to assign roles to registered users in CTIS
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CTIS Video Tutorial – Managing a Clinical Trial in CTIS: Trial & Recruitment Notices (Sponsor)

CTIS Video Tutorial – Managing a Clinical Trial in CTIS: Trial & Recruitment Notices (Sponsor)

Training module: How to

CTIS Video Tutorial – Creating a Clinical Trial: Trial-Centric vs Organisation-Centric Approach

CTIS Video Tutorial – Creating a Clinical Trial: Trial-Centric vs Organisation-Centric Approach

Training module:

CTIS Video Tutorial – Managing a Clinical Trial in CTIS Sponsor Workspace: Other Notifications

CTIS Video Tutorial – Managing a Clinical Trial in CTIS Sponsor Workspace: Other Notifications

Training module: How to

CTIS Video Tutorial - How to manage the workload in CTIS - Timetable

CTIS Video Tutorial - How to manage the workload in CTIS - Timetable

Training module: Support with workload

CTIS Video Tutorial - How to manage the workload in CTIS - RFI tab (sponsor workspace)

CTIS Video Tutorial - How to manage the workload in CTIS - RFI tab (sponsor workspace)

Training module: Support with workload

CTIS Video Tutorial - How to create, cancel or clear, and submit an annual safety report

CTIS Video Tutorial - How to create, cancel or clear, and submit an annual safety report

Training module: How to create and submit an Annual Safety Report and respond to related Requests for Information. This

CTIS Video Tutorial - How to submit a substantial modification in the CTIS Sponsor workspace

CTIS Video Tutorial - How to submit a substantial modification in the CTIS Sponsor workspace

Training module: Create, submit and withdraw a clinical trial application (Sponsors). The

CTIS Video Tutorial - How to respond to RFI considerations and submit an RFI response

CTIS Video Tutorial - How to respond to RFI considerations and submit an RFI response

Training module: How to respond to RFIs received during the evaluation of a Clinical Trial Application. This

CTIS Video Tutorial - CTIS specific functionalities

CTIS Video Tutorial - CTIS specific functionalities

Training module: Overview of

CTIS Bitesize talk

CTIS Bitesize talk

... through uh

Preparing Content for CTIS & the EU CTR

Preparing Content for CTIS & the EU CTR

The second

CTIS Video Tutorial - How to request roles and how to assign roles to registered users in CTIS

CTIS Video Tutorial - How to request roles and how to assign roles to registered users in CTIS

Training module:

Clinical Trials Information System Demonstration for CTIS stakeholders – part 2- January 2022

Clinical Trials Information System Demonstration for CTIS stakeholders – part 2- January 2022

Notifications and supervision activities 00:00