Transition Your Clinical Trials to CTIS

(36)

CRA Basics: The Clinical Trials Information System CTIS

(3:25)

Clinical Trials Information System CTIS bitesize talk: Initial clinical trial application

(1:29:43)

Clinical Trials Information System (CTIS) bitesize talk: User access and role management

(1:25:48)

Webinar for SMEs and Academia on CTR/CTIS

(3:34:57)

Clinical Trials Information System (CTIS): Walk-in clinic

(47:17)

Clinical Trials Information System Demonstration for CTIS stakeholders – part 1

(3:41:40)

Clinical Trials Information System Demonstration for CTIS stakeholders – part 2

(2:59:36)

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

(3:35)

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)

Webinar on transparency rules for the EU Clinical Trials Information System CTIS

(1:7:39)

CTIS – M08 How to assess an initial clinical trial application in CTIS – Part II

(4:43)

Clinical Trials Information System (CTIS): Walk-in clinic

(47:21)

Clinical Trials Information System (CTIS) bitesize talk: Notifications - Part 1

(1:27:14)

CTR / CTIS go-live press briefing 25 January 2022

(40:15)

Interview: Clinical Trials Information System - CTIS - First Experiences

(16:6)

CTIS Bitesize Talk: Annual safety report (ASR) – 15 Dec 2022

(1:29:11)