CTIS - M12 Data protection in CTIS

(5:10)

Clinical Trials Information System Demonstration for CTIS stakeholders – part 2

(2:59:36)

Webinar for SMEs and Academia on CTR/CTIS

(3:34:57)

CTIS – M10 How to submit an initial CTA in the CTIS – Fill in the Part II section

(5:20)

Handling | M12

(2:39)

CTIS – M07 How to create a CT: Clinical Trial centric approach vs organisation centric approach

(3:)

Interview: Impact of CTIS on TMF Management

(27:45)

CTIS - M06 How to access an initial CTA in CTIS – RMS selection

(5:30)

CTIS – M10 How to submit an initial CTA in the CTIS – Fill in the Sponsor details of Part I section.

(4:)

CTIS – M11 How to access and view an RFI in CTIS (Sponsors)

(2:38)

CTIS - M15 How to view and download CTs in the authority workspace

(5:30)

CTIS - M11 How to respond to RFI considerations and submit an RFI response (Sponsors)

(3:35)

CTIS - M14 How to create and cancel a Corrective Measure (Authority)

(7:6)

CTIS – M05 How to manage a clinical trial in the CTIS sponsor workspace – Other notifications

(4:23)

CTIS - M02 CTIS Public Website

(2:6)

CTIS - M17 How to update and complete an ad hoc assessment

(3:57)

CTIS - M02 CTIS Specific Functionalities

(3:30)

CTIS Bitesize talk: Deferral rules and Public website

(1:28:56)

CTIS - M03 Registration of a new organisation in CTIS

(3:22)